EP1546335A2 - Manipulation genetique de tannins condens s - Google Patents

Manipulation genetique de tannins condens s

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Publication number
EP1546335A2
EP1546335A2 EP03762203A EP03762203A EP1546335A2 EP 1546335 A2 EP1546335 A2 EP 1546335A2 EP 03762203 A EP03762203 A EP 03762203A EP 03762203 A EP03762203 A EP 03762203A EP 1546335 A2 EP1546335 A2 EP 1546335A2
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European Patent Office
Prior art keywords
plant
seq
ban
coding sequence
polypeptide
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EP03762203A
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German (de)
English (en)
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EP1546335A4 (fr
EP1546335B1 (fr
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Richard A. Dixon
Nancy L. Paiva
Deyu Xie
Shashi Sharma
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Roberts Samuels Noble Foundation Inc
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Roberts Samuels Noble Foundation Inc
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    • C—CHEMISTRY; METALLURGY
    • C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12N—MICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
    • C12N9/00—Enzymes; Proenzymes; Compositions thereof; Processes for preparing, activating, inhibiting, separating or purifying enzymes
    • C12N9/0004—Oxidoreductases (1.)
    • C12N9/0006—Oxidoreductases (1.) acting on CH-OH groups as donors (1.1)
    • C—CHEMISTRY; METALLURGY
    • C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12N—MICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
    • C12N15/00—Mutation or genetic engineering; DNA or RNA concerning genetic engineering, vectors, e.g. plasmids, or their isolation, preparation or purification; Use of hosts therefor
    • C12N15/09—Recombinant DNA-technology
    • C12N15/63—Introduction of foreign genetic material using vectors; Vectors; Use of hosts therefor; Regulation of expression
    • C12N15/79—Vectors or expression systems specially adapted for eukaryotic hosts
    • C12N15/82—Vectors or expression systems specially adapted for eukaryotic hosts for plant cells, e.g. plant artificial chromosomes (PACs)
    • C12N15/8241—Phenotypically and genetically modified plants via recombinant DNA technology
    • C12N15/8242—Phenotypically and genetically modified plants via recombinant DNA technology with non-agronomic quality (output) traits, e.g. for industrial processing; Value added, non-agronomic traits
    • C12N15/8243—Phenotypically and genetically modified plants via recombinant DNA technology with non-agronomic quality (output) traits, e.g. for industrial processing; Value added, non-agronomic traits involving biosynthetic or metabolic pathways, i.e. metabolic engineering, e.g. nicotine, caffeine
    • C—CHEMISTRY; METALLURGY
    • C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12N—MICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
    • C12N15/00—Mutation or genetic engineering; DNA or RNA concerning genetic engineering, vectors, e.g. plasmids, or their isolation, preparation or purification; Use of hosts therefor
    • C12N15/09—Recombinant DNA-technology
    • C12N15/63—Introduction of foreign genetic material using vectors; Vectors; Use of hosts therefor; Regulation of expression
    • C12N15/79—Vectors or expression systems specially adapted for eukaryotic hosts
    • C12N15/82—Vectors or expression systems specially adapted for eukaryotic hosts for plant cells, e.g. plant artificial chromosomes (PACs)
    • C12N15/8241—Phenotypically and genetically modified plants via recombinant DNA technology
    • C12N15/8242—Phenotypically and genetically modified plants via recombinant DNA technology with non-agronomic quality (output) traits, e.g. for industrial processing; Value added, non-agronomic traits
    • C12N15/8243—Phenotypically and genetically modified plants via recombinant DNA technology with non-agronomic quality (output) traits, e.g. for industrial processing; Value added, non-agronomic traits involving biosynthetic or metabolic pathways, i.e. metabolic engineering, e.g. nicotine, caffeine
    • C12N15/825—Phenotypically and genetically modified plants via recombinant DNA technology with non-agronomic quality (output) traits, e.g. for industrial processing; Value added, non-agronomic traits involving biosynthetic or metabolic pathways, i.e. metabolic engineering, e.g. nicotine, caffeine involving pigment biosynthesis

Definitions

  • the present invention generally relates to plant genetics. More specifically, the invention relates to genes involved in the biosynthesis of condensed tannins, and methods for use thereof.
  • CTs Condensed tannins
  • Flavan-3-ol fiavonoid units
  • CTs are also commonly termed proanthocyanidins due to the red anthocyanidins that are produced upon heating in acidic alcohol solutions.
  • the most common anthocyanidins produced are cyanidin (from procyanidin) and delphinidin (from prodelphinidin).
  • CTs may contain from 2 to 50 or more fiavonoid units.
  • CT polymers have complex structures because of variations in the fiavonoid units and the sites for interflavan bonds. Depending on their chemical structure and degree of polymerization, CTs may or may not be soluble in aqueous organic solvents.
  • CTs are attracting increasing attention due to their ability to affect the nutritional quality of human and animal food (Bagchi et al, 2000; Barry and McNabb, 1999; Morris and Robbins, 1997).
  • CTs from various plants have beneficial effects on cardiac health and immune responses (Pataki et al, 2002; Foo et al, 2000; Lin et al, 2002). They can reversibly bind to proteins and reduce their degradation rate.
  • the presence of moderate amounts of CT in forage crops reduces the initial rate of microbial digestion of the protein component of forage material in the rumen.
  • CTs In Arabidopsis thaliana, CTs accumulate predominantly in the endothelium layer of the seed coat. Many mutations that affect the seed coat color and CT accumulation have been characterized and the corresponding genes cloned. These genes include BAN (Genbank Accession No. AF092912; Devic et al, 1999), TTG1 TTG2, TT1, TT2, TT8 and TT12. The ban mutation leads to accumulation of anthocyanins in the seed coat instead of CTs.
  • TTG1, TTG2, TT1, TT2 and TT8 are regulatory genes and encode a WD-repeat protein (Walker et al, 1999), a WRKY family protein, a WTP subfamily plant zinc finger protein (Sagasser et al, 2002), an R2R3 MYB domain protein (Nesi et al, 2001) and a basic helix-loop-helix domain protein (Nesi et al, 2000), respectively.
  • Expression of the TT2 gene has been shown to induce the TT8 and BAN genes but does not lead to accumulation of CT (Nesi et al, 2001). All the above genes are predominantly expressed in the seed coat endothelium.
  • the BAN gene encodes an apparent biosynthetic enzyme with sequence similarity to dihydroflavonol reductase (DFR) (Devic et al, 1999), whereas the TT12 gene encodes a multidrug secondary transporter-like protein that may be required for sequestration of fiavonoid in vacuoles, the subcellular site of CT deposition (Debeaujon et al, 2001). It has been suggested that the BAN gene might encode an LAR, based on its sequence similarity to DFR and the loss of CT in the ban mutation (Devic et al, 1999).
  • the invention provides an isolated nucleic acid sequence encoding a BAN polypeptide.
  • a nucleic acid sequence may, in certain embodiments of the invention, be further defined as comprising a nucleic acid sequence selected from the group consisting of: a) a nucleic acid sequence encoding the polypeptide of SEQ LD NO:2, b) a nucleic acid sequence comprising the sequence of SEQ ID NO:l; and c) a nucleic acid sequence hybridizing to SEQ LD NO:l under high stringency conditions and having BAN activity.
  • the sequence may also be operably linked to a heterologous promoter and/or a heterologous terminator.
  • an isolated polypeptide comprising the amino acid sequence of SEQ ID NO:2.
  • the invention provides a transgenic plant transformed with a selected DNA comprising a coding sequence encoding a BAN polypeptide.
  • the polypeptide comprises the sequence of SEQ LD NO:2 and/or SEQ LD NO:4.
  • the selected DNA encodes a BAN polypeptide comprising a sequence selected from the group consisting of SEQ ID NO:2, SEQ ID NO:4, SEQ ID NO:30, SEQ ID NO:32, SEQ JD NO:34, SEQ LD NO:36, SEQ LD NO:38, SEQ LD NO:40, SEQ JD NO:42, SEQ ID NO:44 and SEQ JD NO:46.
  • the coding sequence may be further defined as comprising the nucleic acid sequence of SEQ ID NO:l or SEQ LD NO:3.
  • the coding sequence may, in further embodiments of the invention, be operably linked to a heterologous promoter and/or a heterologous terminator.
  • the selected DNA may also comprise an enhancer, plasmid DNA, and/or a signal peptide.
  • the transgenic plant may be a monocotyledonous or dicotyledonous plant. Examples of monocotyledonous plants include wheat, maize, rye, rice, oat, barley, turfgrass, sorghum, millet and sugarcane.
  • Examples of dicotyledonous plants include tobacco, tomato, potato, soybean, cotton, canola, alfalfa, sunflower, and cotton.
  • the plant is maize. In another embodiment of the invention, the plant is an alfalfa plant.
  • a transgenic plant prepared in accordance with the invention may further comprise a transgenic coding sequence encoding the chalcone isomerase polypeptide encoded by SEQ JD NO:25, SEQ JD NO:26, SEQ JD NO:27 and or SEQ JD NO:28.
  • the transgenic plant comprises a coding sequence encoding the polypeptide of SEQ JD NO: 16, SEQ JD NO: 18, SEQ LD NO:20, SEQ JD NO:22 and/or SEQ JD NO:24.
  • a transgenic plant in accordance with the invention may, in one embodiment of the invention, be further defined as a fertile R 0 transgenic plant, and may also be a progeny plant of any generation of a fertile R 0 transgenic plant, wherein said transgenic plant has inherited said selected DNA from said Ro transgenic plant.
  • the invention also provides a seed of such a transgenic plant, wherein said seed comprises said selected DNA.
  • the invention provides a method of increasing tannin biosynthesis in a plant, comprising introducing into said plant a selected DNA comprising a coding sequence encoding the polypeptide of SEQ JD NO:2 and/or SEQ JD NO:4 operably linked to a promoter functional in said plant.
  • increased or increasing it is understood in the art that it is meant that a statistically significant increase has been made, e.g., P>0.10 and preferably P>0.05 from tannin production and/or content increase relative to a corresponding plant not increased for tannin biosynthesis.
  • the coding sequence encodes the polypeptide of SEQ JD NO:2 or SEQ JD NO:4, and may be further defined as comprising the nucleic acid sequence of SEQ LD NO:l or SEQ JD NO:3.
  • the coding sequence encodes a polypeptide selected from the group consisting of SEQ JD NO:2, SEQ ID NO:4, SEQ ID NO:30, SEQ JD NO:32, SEQ JD NO:34, SEQ LD NO:36, SEQ JD NO:38, SEQ JD NO:40, SEQ JD NO:42, SEQ JD NO:44 and SEQ ID NO:46.
  • the coding sequence may, in certain embodiments of the invention, be operably linked to one or more heterologous regulatory elements, including a heterologous promoter, terminator or enhancer.
  • Introducing the selected DNA may be carried out by any method, including by backcrossing and genetic transformation with said selected DNA.
  • the selected DNA may also comprise a sequence encoding a signal peptide.
  • a promoter used may be any type of promoter, including a constitutive or tissue specific promoter.
  • the plant may be a monocotyledonous or dicotyledonous plant.
  • monocotyledonous plants include wheat, maize, rye, rice, oat, barley, turfgrass, sorghum, millet and sugarcane.
  • dicotyledonous plants include tobacco, tomato, potato, soybean, cotton, canola, alfalfa, sunflower, and cotton. Jn one embodiment of the invention the plant is maize. In another embodiment of the invention the plant is an alfalfa plant.
  • the method may further comprise preparing a transgenic progeny plant of any generation comprising said selected DNA.
  • the invention further provides a plant prepared in accordance with any of the methods of the invention.
  • the invention provides a method of making food for human or animal consumption comprising: (a) obtaining a plant prepared in accordance with the invention;
  • the invention provides a method for modifying the pigmentation of a plant comprising introducing into said plant a selected DNA comprising a coding sequence encoding the polypeptide of SEQ ID NO:2 and/or SEQ JD NO:4 operably linked to a promoter functional in said plant, wherein the expression of said coding sequence results in a decrease in anthocyanin pigmentation in the plant relative to a second plant that only differs from said plant in that said selected DNA is absent in the second plant.
  • the coding sequence encodes a polypeptide selected from the group consisting of SEQ LD NO:2, SEQ JD NO:4, SEQ JD NO:30, SEQ JD NO:32, SEQ ID NO:34, SEQ JD NO:36, SEQ JD NO:38, SEQ JD NO:40, SEQ JD NO:42, SEQ JD NO:44 and SEQ ID NO:46.
  • "decrease” means a statistically significant difference in anthocyanin concentration and/or visual detection (e.g., p>0.10 and preferably P>0.05).
  • the coding sequence comprised the nucleic acid sequence of SEQ ID NO:l or SEQ ID NO:3.
  • the coding sequence may, in one embodiment of the invention, be operably linked to one or more heterologous regulatory elements, including a heterologous promoter, terminator or an enhancer.
  • Introducing the selected DNA may be carried out by any method, including by backcrossing and genetic transformation with said selected DNA.
  • the selected DNA may also comprise a sequence encoding a signal peptide.
  • a promoter used may be any type of promoter, including a constitutive or tissue specific promoter.
  • the method may comprise production of plants wherein any and/or all parts of the plant have modified pigmentation.
  • the flowers, seed coat and/or leaves comprise decreased anthocyanin pigmentation.
  • the plant may be a monocotyledonous or dicotyledonous plant.
  • monocotyledonous plants include wheat, maize, rye, rice, oat, barley, turfgrass, sorghum, millet and sugarcane.
  • dicotyledonous plants include tobacco, tomato, potato, soybean, cotton, canola, alfalfa, sunflower, and cotton.
  • the plant is maize.
  • the plant is an alfalfa plant.
  • the method may further comprise preparing a transgenic progeny plant of any generation comprising said selected DNA.
  • the invention further provides a plant prepared in accordance with any of the methods of the invention. BRIEF DESCRIPTION OF THE DRAWINGS
  • FIG. 1 Shows the published proposed biosynthetic pathways leading to anthocyanins and condensed tannins.
  • PAL phenylalanine ammonia-lyase
  • C4H cinnamate-4-hydroxylase
  • 4CL 4-coumaroyl:CoA-ligase
  • CHS chalcone synthase
  • F3H flavanone 3-hydroxylase
  • F3'H fiavonoid 3' hydroxylase
  • F3'5'H fiavonoid 3'5'hydroxylase
  • DFR dihydroflavonol 4- reductase
  • LAR leucoanthocyanidin reductase
  • CON condensing enzyme(s).
  • FIG. 2 Shows the analysis o ⁇ Arabidopsis thaliana BAN gene expression in leaves of transgenic Arabidopsis plants by RT-PCR.
  • the numbers refer to independent transformants harboring the 2x35S::BAN gene construct.
  • +C plasmid carrying the Arabidopsis BAN gene used as positive control;
  • -C total RNA from a plant transformed with empty vector;
  • M molecular size markers.
  • FIG. 3 Shows RT-PCR analysis of transgenic Arabidopsis plants harboring both the T- DNA activation tagged PAP1-D gene and the Arabidopsis BAN transgene, which have lost anthocyanin pigmentation for the expression of PAP1-D, BAN and actin mRNA.
  • FIG. 4 Shows the tissue specificity of endogenous BAN gene expression in Medicago truncatula determined by RT-PCR (A) and Northern blot (B).
  • NRSUFL non-red-spot-unfolded leaves
  • NRSFL non-red-spot-folded leaves
  • RSUFL red-spot-unfolded leaves
  • RSFL red-spot- folded leaves
  • FB flower buds
  • OF open flowers
  • 16RT 16-day old geminated roots
  • 4WNRT 4-week old nodulated roots
  • DGH dark-grown hypocotyls
  • 30LH 30-hour light-induced hypocotyls
  • 50LH 50-hour light-induced hypocotyls
  • YS young seeds.
  • FIG. 7 Shows flower petal coloration for wild-type and BAN transgenic tobacco plants.
  • the plants were: 1, wild-type; 2, B-ll; 3, B-17-A; 4, B-19-A; 5, B-21-B; 6, 121-3-A (empty vector control); 7, D-5-C (a transgenic plant over-expressing an M. truncatula dihydroflavonol reductase transgene).
  • FIG. 8 Shows the presence of CTs in petals of transgenic tobacco expressing M. truncatula BAN (3 and 4) in comparison with petals from wild-type plants (1 and 2). Petals were stained with 0.1% DMACA in ethanol/6M HCI (1:1)
  • FIG. 9 Shows the levels of anthocyanins in petals of tobacco plants expressing the M. truncatula BAN gene (lines designated with B-) compared to empty vector control lines (121- designation) or wild-type plants (CK- designation). Anthocyanins were extracted in ethanolic HCI, and their levels determined by measurement of absorbance at 528 nm.
  • FIG. 10 MtBAN catalyzes the conversion of cyanidin into catechin and epicatechin.
  • FIG 11 Comparison of UN spectra of ( ⁇ )catechin (A) and (-)epicatechin (B) standards and enzymatic products of MtBA ⁇ acting on cyanidin (C, 19.6 min product, putative catechin and D, 31.9 min product, putative epicatechin)
  • FIG. 12 MtBA ⁇ catalyzes the conversion of pelargonidin into afzelechin.
  • A reaction products from MtBA ⁇ enzyme extract, with putative epiafzelechin peak labeled;
  • B pSE380 vector control enzyme extract;
  • C boiled MtBA ⁇ enzyme extract;
  • D boiled ⁇ SE380 vector control enzyme extract.
  • FIG. 13 UN spectrum of putative epiafzelechin peak.
  • FIG. 14 MtBAN catalyzes the conversion of delphinidin into gallocatechin and epi- gallocatechin.
  • Gallocatechin (A) and epi-gallocatechin (B) standards reaction products from MtBAN enzyme extract (C); pSE380 vector control enzyme extract (D); boiled MtBAN enzyme (E).
  • FIG. 15 Comparison of UN spectra of (-)gallocatechin (A) and (-)epi-gallocatechin (B) standards and BA ⁇ -enzymatic products (1:C and 2:D). and enzymatic products of MtBA ⁇ acting on delphinidin (C, 9.6 min product, putative (-)gallocatechin and D, 18.8 min product, putative (-) epi-gallocatechin )
  • FIG. 16A-D AtBA ⁇ catalyzes the conversion of cyanidin into epi-catechin. ⁇ ADPH was used as coenzyme.
  • FIG. 16 A reaction products from AtBA ⁇ enzyme extract
  • FIG. 16B boiled AtBA ⁇ enzyme extract
  • FIG. 16C vector control enzyme extract
  • FIG. 16D epicatechin standard.
  • FIG. 17A-B Comparison of UN spectra of epi-catechin standard (FIG. 17A) and the AtBA ⁇ enzyme reaction product, putative epi-catechin (FIG. 17B).
  • FIG. 18A, 18B, 18C AtBA ⁇ catalyzes the conversion of pelargonidin into epiafzelechin, ⁇ ADPH used as coenzyme.
  • FIG. 18 A reaction products from BAN enzyme extract
  • FIG. 18B boiled enzyme extraction
  • FIG. 18C vector control enzyme extraction.
  • FIG. 19 UN spectrum of AtBA ⁇ enzymatic reaction product, putative epiafzelechin
  • FIG. 20 AtBA ⁇ catalyzes the conversion of delphinidin into gallocatechin, ⁇ ADPH used as coenzyme.
  • A reaction products from BAN enzyme extract; B, boiled enzyme extract; C, vector control enzyme extract.
  • FIG. 21 UV spectrum of AtBAN enzyme reaction product, putative gallocatechin.
  • FIG. 22 Schematic presentation of BAN catalyzing the conversion (anthocyanin reductase reaction) of cyanidin into epicatechin and catechin
  • FIG. 23 Proposed modified condensed tannins biosynthetic pathway.
  • ANR (BAN) catalyzes the conversion of anthocyanidins into flavan-3-ols which are then inco ⁇ orated into condensed tannins.
  • PAL phenylalanine ammonia-lyase
  • C4H cinnamate-4-hydroxylase
  • 4CL 4-coumaroyl:CoA-ligase
  • CHS chalcone synthase
  • F3H flavanone 3-hydroxylase
  • F3'H fiavonoid 3' hydroxylase
  • F3'5'H fiavonoid 3'5'hydroxylase
  • DFR dihydroflavonol 4- reductase
  • LAR leucoanthocyanidin reductase
  • ANS anthocyanidin synthase
  • ANR Anthocyanidin reductase (BAN); CON: condensing enzyme(s).
  • FIG. 24 Alignment of BAN coding sequence open reading frames. Shown are sequences from Arabidopsis: At BAN1 (SEQ JD NO:3), At BAN 2 (SEQ JD NO:47); barley: Barley306 (SEQ ED NO:29), Barley316 (SEQ ID NO: 31), Barley49014 (SEQ JD NO:33), Barley55701 (SEQ JD NO:35); Brassica napus (SEQ JD NO:37); cotton: Cotton4107 (SEQ ID NO:39); grape: Grape4226 (SEQ ID NO:41); M. truncatula: Medicago90858 (SEQ ID NO:l); and sorghum: Sorghum34457 (SEQ JD NO:43), Sorghum34925 (SEQ JD NO:45).
  • FIG. 25 Alignment of BAN polypeptides. Shown are polypeptides from Arabidopsis: At BAN1 (SEQ JD NO:4), At BAN 2 (SEQ JD NO:48); barley: Barley306 (SEQ JD NO:30), Barley316 (SEQ JD NO: 32), Barley49014 (SEQ LD NO:35), Barley55701 (SEQ ID NO:37); Brassica napus (SEQ LD NO:39), cotton: Cotton4107 (SEQ LD NO:41); grape: Grape4226 (SEQ ID NO:42); M. truncatula: Medicago90858 (SEQ JD NO:2); and sorghum: Sorghum34457 (SEQ ID NO:44), Sorghum34925 (SEQ JD NO:46).
  • FIG. 26 Anthocyanidin reductase in Lotus corniculatus. HPLC analysis showed that ANR converts cyaniding into epicatechin. a, the incubation of extract with cyanidin and NADPH producing epicatechin (arrow); b, the incubation of boiled extract with cyandin and NADPH; c, authentic standard epicatehin (arrow).
  • FIG. 27 Anthocyanidin reductase in grape fruit skin of Vitis vinifer. a, the incubation of extract with cyanidin and NADPH producing epicatechin (arrow); b, the incubation of boiled extract with cyandin and NADPH; c, authentic standard epicatehin (arrow).
  • FIG. 28 Anthocyanidin reductase in testa tissue of Hordeum vulgera (barley) cv. morex. a, the incubation of extract with cyanidin and NADPH producing epicatechin (arrow); b, the incubation of boiled extract with cyandin and NADPH; c, authentic standard epicatehin (arrow).
  • FIG. 29A-D Anthocyanidin reductase (ANR) in different tissues of Desmodium uncinatum.
  • FIG. 29 A ANR from flowers; a, the incubation of extract with cyanidin and NADPH producing epicatechin (arrow); b, the incubation of boiled extract with cyandin and NADPH; c, authentic standard epicatehin (arrow).
  • FIG. 29B ANR from leaves; a, the incubation of extract with cyanidin and NADPH producing epicatechin (arrow); b, the incubation of boiled extract with cyandin and NADPH; c, authentic standard epicatehin (arrow).
  • FIG. 29 A ANR from flowers; a, the incubation of extract with cyanidin and NADPH producing epicatechin (arrow); b, the incubation of boiled extract with cyandin and NADPH; c, authentic standard epicatehin (arrow).
  • FIG. 29 A ANR from flowers; a, the incubation of extract
  • FIG. 29C ANR from young pods; a, the incubation of extract with cyanidin and NADPH producing epicatechin (arrow); b, the incubation of boiled extract with cyandin and NADPH; c, the incubation of buffer and extract without NADPH and cyanidin; d, authentic standard epicatehin (arrow).
  • FIG. 29D barley extract has ANR inhibitor; a, the incubation of extracts from pods with cyanidin and NADPH producing epicatechin (arrow); b, the incubation of extract from pods and barley testa with cyanidin and NADPH producing less epicatechin (arrow).
  • the invention overcomes the limitations of the prior art by providing methods and compositions for the modification of condensed tannin (CT) metabolism in plants.
  • CT condensed tannin
  • the invention has numerous important applications to agriculture.
  • One important advance of the invention is that it allows, for the first time, the production of CT in plants or plant tissues that otherwise lack significant CT content.
  • introduction of a transgene encoding a CT biosynthesis gene into a plant otherwise lacking the gene, or of a gene that is present in the plant but is expressed in minimal quantity in a given plant tissue the production and accumulation of CT can be induced.
  • CT can counter this by reversibly binding to proteins to reduce their degradation rate.
  • the presence of moderate amounts of CT in forage crops reduces the initial rate of microbial digestion of the protein component of forage material in the rumen.
  • CTs protein-tannin complexes then pass to the abomasum where they dissociate at the lower pH, providing "by-pass protein" for utilization by the animal and consequent enhancement of milk and wool production and live weight gain.
  • the reduced protein degradation that occurs in the presence of CTs helps protect against bloat (Tanner et al., 1995).
  • CTs also preserve proteins during the ensiling process, increasing the feed value of silage and reducing the amount of nitrogen that is lost to the environment as feedlot waste (Albrecht and Muck, 1991; Reed, 1995).
  • CT modification could be engineered into feed components that are blended or added to bloat-causing components to reduce the bloat incidence in animals consuming the mixed feed.
  • One application of the invention is thus the modification of CT biosynthesis in plants with low CT content.
  • Alfalfa is one such plant. Condensed tannins are made in alfalfa (Medicago sativa), as in Arabidopsis, in the seed coat, but do not accumulate in the leaves (Koupai-Abyazani et al, 1993; Skadhauge et al, 1997). Nonetheless, alfalfa is the world's major forage legume. Therefore, introducing CT biosynthesis to the leaves or other tissues of alfalfa or other low CT plants would substantially improve the utility of this crop for feed by reduction of its potential for causing pasture bloat. Forage crops that accumulate CTs in leaves have low bloating potential; these include Lotus corniculatus, Leucaena leucocephala, Hedysarum sulfurescens and Robinia spp.
  • the present invention provides a gene from Medicago truncatula encoding an enzyme that functions to direct precursor from the anthocyanin pathway into the formation of condensed tannins. Also disclosed are methods for the genetic manipulation of condensed tannins for constitutive production of these compounds in plants for a variety of uses.
  • CTs are synthesized in plants by the fiavonoid branch of the phenylpropanoid pathway.
  • the first dedicated step in the CT-specific branch pathway has been believed to be the conversion of leucoanthocyanidin, an intermediate also involved in anthocyanin biosynthesis, into catechin by a putative leucoanthocyanidin reductase (LAR) (FIG. 1). Catechins and leucoanthocyanidins are then transported into the vacuole, where they polymerize into CTs. The mechanism of polymerization is completely unknown.
  • one application of the invention is the introduction or increase of condensed tannin biosynthesis in plants. Such applications may result in forage improvement and nutritional improvement of foods. While much of the fiavonoid pathway leading to condensed tannins may be present in a number of tissues, especially those accumulating anthocyanins, the LAR step or another unknown step is critical to formation of condensed tannin monomers (flavan-3-ols) such as catechin and epicatechin, and this step appears to be lacking in tissues which do not accumulate condensed tannins. As such, expression of the LAR step and/or potentially other steps may be used for increasing CT biosynthesis.
  • condensed tannin monomers flan-3-ols
  • Tobacco flower data provided herein demonstrate the utility of the approach using the Medicago truncatula BAN clone, since it increased condensed tannins and decreased anthocyanin content (as predicted based on pathway competition).
  • Arabidopsis BAN was also shown to increase condensed tannins in Arabidopsis when over-expressed.
  • the invention may also be used to improve the nutritional quality of a plant.
  • Catechins and similar flavonoids have been reported to behave as strong antioxidants and have other properties which may make their consumption beneficial to human and animal health.
  • such compounds are generally antimicrobial, and their presence may improve food quality by preventing pre- and post-harvest damage. Accordingly, increases in CT biosynthesis may be used to achieve the associated health benefits.
  • Another use of the invention comprises the alteration of pigmentation in plant parts, including, but not limited to, flower color, seed coat color and leaf color. This can be achieved, for example, by decreasing anthocyanin content via over-expression of BAN, thereby preventing anthocyanin accumulation and the associated pigmentation of plant tissue. Accumulation of the products of BAN (flavan-3-ols, such as catechin(s), condensed tannins, or similar compounds) may simultaneously improve the nutritional, disease resistance, or herbivore resistance of the plant products.
  • seed coat color can be modified.
  • White soybean seed coats are desirable in many markets, and are generally obtained using a certain germplasm source which confers low CHS activity on seed coats. Soybean breeders are thus interested in alternative traits to manipulate seed color. The invention provides a means of such manipulation.
  • the invention further provides two Medicago truncatula dihydroflavonol reductase (DFR) clones that were isolated from young developing Medicago truncatula seeds, which were shown to accumulate condensed tannins in their seed coats (SEQ JD NO:5; SEQ JD NO: 6), or a BAN homolog from Medicago truncatula (SEQ JD NO:7).
  • DFR Medicago truncatula dihydroflavonol reductase
  • upstream e.g., F3H or F3 ⁇
  • downstream e.g., LAR/BAN
  • the two Medicago truncatula DFR clones exhibit different kinetic properties in in vitro enzyme assays, and these properties may reflect different roles in metabolism in the cell. They also showed subtle differences in mRNA accumulation in different tissues, suggesting multiple roles or the presence of multiple pathways at work in the same tissue.
  • the genes may thus find use as part of a combination of genes to introduce or increase condensed tannin biosynthesis in numerous species, for forage improvement and nutritional improvement of foods.
  • CT expression could also be modulated using a transgenic chalcone isomerase coding sequence (McKhann and Hirsch, 1994; SEQ JD NO:25; SEQ JD NO:26; SEQ JD NO:27; SEQ JD NO:28).
  • Medicago chalcone isomerase increases fiavonoid biosynthesis in Arabidopsis (x3).
  • This could thus be used in combination with BAN to produce more CT.
  • An Arabidopsis or other PAP-1 gene could also be used to increase flux into pathway (Borevitz, 2000; SEQ JD NO: 15).
  • BAN could also be used in conjunction with other regulatory genes such as TTGl (GenBank Accession No. AJl 33743; SEQ JD NO: 19, SEQ ID NO:20), TTG2, TT1 (GenBank Accession No.
  • AF190298 SEQ JD NO:23, SEQ JD NO:24
  • TT2 Nesi et al, 2001
  • TT8 Genesi et al, 2001
  • Benefit may also be obtained from use of BAN in conjunction with TT12 (GenBank Accession No. AJ294464; SEQ ID NO: 21, SEQ JD NO:22) for transport of monomers to the vacuole.
  • the invention also provides BAN sequences that were originally identified from the plant species barley (SEQ JD NO:29, SEQ JD NO:31, SEQ JD NO:33 and SEQ JD NO:35), sorghum (SEQ ID NO:43 and SEQ JD NO:45), Brassica napus (SEQ JD NO:37), cotton (SEQ JD NO:39) and grape (SEQ ID NO:41).
  • the corresponding polypeptides encoded are given in SEQ JD NO:30, SEQ JD NO:32, SEQ JD NO:34, SEQ JD NO:36, SEQ JD NO:38, SEQ JD NO:40 and SEQ JD NO:42.
  • nucleic acids thus comprises these nucleic acids and nucleic acids encoding the foregoing polypeptides, as well as the use thereof for plant transformation. Also provided are nucleic acids hybridizing to any of the foregoing nucleic acid sequences and encoding a polypeptide having BAN activity.
  • a modulation of the phenotype of a gene may be obtained in accordance with the invention by administering a recombinant nucleic acid sequence containing a BAN coding sequence.
  • a nucleic acid may be present as a sense and/or antisense nucleic acid.
  • Provided by the invention are BAN sequences which hybridize to the coding sequences provided herein under high stringency conditions.
  • “hybridization” or “hybridizes” is understood to mean the forming of a double or triple stranded molecule or a molecule with partial double or triple stranded nature.
  • stringent condition(s)” or “high stringency” are those conditions that allow hybridization between or within one or more nucleic acid strand(s) containing complementary sequence(s), but precludes hybridization of random sequences.
  • Medium stringent conditions tolerate little mismatch between a nucleic acid and a target strand. Such conditions are well known to those of ordinary skill in the art, and are preferred for applications requiring high selectivity.
  • Medium stringent conditions may comprise relatively low salt and/or relatively high temperature conditions, such as provided by about 5X SSC, 50% formamide and 42°C; or alternatively, 5X SSC, 50% formamide and 55°C.
  • High stringency may be defined as 0.02M to 0.10M NaCl and 50°C to 70°C. Specific examples of such conditions include 0.02M NaCl and 50°C; 0.02M NaCL and 60°C; and 0.02M NaCL and 70°C.
  • the temperature and ionic strength of a desired stringency are determined in part by the length of the particular nucleic acid(s), the length and nucleobase content of the target sequence(s), the charge composition of the nucleic acid(s), and to the presence or concentration of formamide, tetramethylammonium chloride or other solvent(s) in a hybridization mixture. It is also understood that compositions and conditions for hybridization are mentioned by way of non-limiting examples only, and that the desired stringency for a particular hybridization reaction in a plant cell is often determined empirically by comparison to one or more positive or negative controls. Depending on the application envisioned it is preferred to employ varying conditions of hybridization to achieve varying degrees of selectivity of a nucleic acid towards a target sequence.
  • one aspect of the current invention is a plant transformation vector comprising one or more CT biosynthesis gene, including a BAN, PAP-1, TTGl TTG2, TT1, TT2 and or TT8 gene.
  • Exemplary coding sequences for use with the invention include those encoding the Medicago truncatula BAN polypeptide (SEQ JD NO:2) or the Arabidopsis thaliana BAN polypeptide (SEQ JD NO:4).
  • Such coding sequences may comprise the nucleic acid sequence of SEQ JD NO:l or SEQ JD NO:3.
  • coding sequences are provided operably linked to a heterologous promoter, in either sense or antisense orientation.
  • Expression constructs are also provided comprising these sequences, as are plants and plant cells transformed with the sequences.
  • CT biosynthesis gene may be provided with other sequences.
  • an expressible coding region that is not necessarily a marker coding region is employed in combination with a marker coding region, one may employ the separate coding regions on either the same or different DNA segments for transformation. In the latter case, the different vectors are delivered concurrently to recipient cells to maximize cotransformation.
  • CT biosynthesis coding sequences will often depend on the purpose of the transformation.
  • One of the major purposes of transformation of crop plants is to add commercially desirable, agronomically important traits to the plant.
  • CTs are known to confer many beneficial effects on health, one such trait is increased biosynthesis of tannins.
  • plants may be engineered to decrease synthesis of CT and increase anthocyanin content.
  • Vectors used for plant transformation may include, for example, plasmids, cosmids, YACs (yeast artificial chromosomes), BACs (bacterial artificial chromosomes) or any other suitable cloning system, as well as fragments of DNA therefrom.
  • vector or "expression vector”
  • all of the foregoing types of vectors, as well as nucleic acid sequences isolated therefrom are included. It is contemplated that utilization of cloning systems with large insert capacities will allow introduction of large DNA sequences comprising more than one selected gene. In accordance with the invention, this could be used to introduce genes corresponding to the entire CT biosynthetic pathway into a plant.
  • DNA segments used for transforming plant cells will, of course, generally comprise the cDNA, gene or genes which one desires to introduce into and have expressed in the host cells. These DNA segments can further include structures such as promoters, enhancers, polylirikers, or even regulatory genes as desired.
  • the DNA segment or gene chosen for cellular introduction will often encode a protein which will be expressed in the resultant recombinant cells resulting in a screenable or selectable trait and/or which will impart an improved phenotype to the resulting transgenic plant.
  • this may not always be the case, and the present invention also encompasses transgenic plants incorporating non-expressed transgenes.
  • Preferred components likely to be included with vectors used in the current invention are as follows.
  • Exemplary promoters for expression of a nucleic acid sequence include plant promoter such as the CaMV 35S promoter (Odell et al, 1985), or others such as CaMV 19S (Lawton et al, 1987), nos (Ebert et al, 1987), Adh (Walker et al, 1987), sucrose synthase (Yang & Russell, 1990), a-tubulin, actin (Wang et al, 1992), cab (Sullivan et al, 1989), PEPCase (Hudspeth and Grula, 1989) or those associated with the R gene complex (Chandler et al, 1989).
  • plant promoter such as the CaMV 35S promoter (Odell et al, 1985), or others such as CaMV 19S (Lawton et al, 1987), nos (Ebert et al, 1987), Adh (Walker et al, 1987), sucrose synthase (Yang & Russell, 1990), a-tubulin, act
  • Tissue specific promoters such as root cell promoters (Conkling et al, 1990) and tissue specific enhancers (Fromm et al, 1986) are also contemplated to be particularly useful, as are inducible promoters such as ABA- and turgor-inducible promoters.
  • inducible promoters such as ABA- and turgor-inducible promoters.
  • the native promoter of a CT biosynthesis gene is used.
  • the DNA sequence between the transcription initiation site and the start of the coding sequence can also influence gene expression.
  • a particular leader sequence with a transformation construct of the invention.
  • Preferred leader sequences are contemplated to include those which comprise sequences predicted to direct optimum expression of the attached gene, i.e., to include a preferred consensus leader sequence which may increase or maintain mRNA stability and prevent inappropriate initiation of translation. The choice of such sequences will be known to those of skill in the art in light of the present disclosure. Sequences that are derived from genes that are highly expressed in plants will typically be preferred.
  • vectors for use in accordance with the present invention may be constructed to include the ocs enhancer element.
  • This element was first identified as a 16 bp palindromic enhancer from the octopine synthase (ocs) gene of Agrobacterium (Ellis et al, 1987), and is present in at least 10 other promoters (Bouchez et al, 1989). It is proposed that the use of an enhancer element, such as the ocs element and particularly multiple copies of the element, will act to increase the level of transcription from adjacent promoters when applied in the context of plant transformation.
  • CT biosynthesis coding sequences may be introduced under the control of novel promoters or enhancers, etc., or homologous or tissue specific promoters or control elements.
  • Vectors for use in tissue-specific targeting of genes in transgenic plants will typically include tissue-specific promoters and may also include other tissue-specific control elements such as enhancer sequences. Promoters which direct specific or enhanced expression in certain plant tissues will be known to those of skill in the art in light of the present disclosure.
  • rbcS promoter specific for green tissue
  • ocs, nos and mas promoters which have higher activity in roots or wounded leaf tissue
  • a truncated (-90 to +8) 35S promoter which directs enhanced expression in roots
  • an a-tubulin gene that also directs expression in roots.
  • Transformation constructs prepared in accordance with the invention will typically include a 3' end DNA sequence that acts as a signal to terminate transcription and allow for the poly-adenylation of the mRNA produced by coding sequences operably linked to a CT biosynthesis gene.
  • the native terminator of a CT biosynthesis gene is used.
  • a heterologous 3' end may enhance the expression of sense or antisense CT biosynthesis genes.
  • Terminators which are deemed to be particularly useful in this context include those from the nopaline synthase gene of Agrobacterium tumefaciens (nos 3' end) (Bevan et al, 1983), the terminator for the T7 transcript from the octopine synthase gene o ⁇ Agrobacterium tumefaciens, and the 3' end of the protease inhibitor I or II genes from potato or tomato.
  • Regulatory elements such as an Adh intron (Callis et al, 1987), sucrose synthase intron (Vasil et al, 1989) or TMV omega element (Gallie et al, 1989), may further be included where desired.
  • Sequences that are joined to the coding sequence of an expressed gene, which are removed post-translationally from the initial translation product and which facilitate the transport of the protein into or through intracellular or extracellular membranes, are termed transit (usually into vacuoles, vesicles, plastids and other intracellular organelles) and signal sequences (usually to the endoplasmic reticulum, golgi apparatus and outside of the cellular membrane).
  • transit usually into vacuoles, vesicles, plastids and other intracellular organelles
  • signal sequences usually to the endoplasmic reticulum, golgi apparatus and outside of the cellular membrane.
  • translatable mRNA in front of the gene may increase the overall stability of the mRNA transcript from the gene and thereby increase synthesis of the gene product. Since transit and signal sequences are usually post- translationally removed from the initial translation product, the use of these sequences allows for the addition of extra translated sequences that may not appear on the final polypeptide. It further is contemplated that targeting of certain proteins may be desirable in order to enhance the stability of the protein (U.S. Patent No. 5,545,818, incorporated herein by reference in its entirety).
  • vectors may be constructed and employed in the intracellular targeting of a specific gene product within the cells of a transgenic plant or in directing a protein to the extracellular environment. This generally will be achieved by joining a DNA sequence encoding a transit or signal peptide sequence to the coding sequence of a particular gene. The resultant transit, or signal, peptide will transport the protein to a particular intracellular, or extracellular destination, respectively, and will then be post-translationally removed.
  • Marker genes are genes that impart a distinct phenotype to cells expressing the marker protein and thus allow such transformed cells to be distinguished from cells that do not have the marker. Such genes may encode either a selectable or screenable marker, depending on whether the marker confers a trait which one can "select” for by chemical means, i.e., through the use of a selective agent (e.g., a herbicide, antibiotic, or the like), or whether it is simply a trait that one can identify through observation or testing, i.e., by "screening” (e.g., the green fluorescent protein).
  • a selective agent e.g., a herbicide, antibiotic, or the like
  • screening e.g., the green fluorescent protein
  • selectable or screenable markers also are genes which encode a "secretable marker" whose secretion can be detected as a means of identifying or selecting for transformed cells. Examples include markers which are secretable antigens that can be identified by antibody interaction, or even secretable enzymes which can be detected by their catalytic activity.
  • Secretable proteins fall into a number of classes, including small, diffusible proteins detectable, e.g., by ELISA; small active enzymes detectable in extracellular solution (e.g., -amylase, ⁇ -lactamase, phosphinothricin acetyltransferase); and proteins that are inserted or trapped in the cell wall (e.g., proteins that include a leader sequence such as that found in the expression unit of extensin or tobacco PR-S).
  • small, diffusible proteins detectable e.g., by ELISA
  • small active enzymes detectable in extracellular solution e.g., -amylase, ⁇ -lactamase, phosphinothricin acetyltransferase
  • proteins that are inserted or trapped in the cell wall e.g., proteins that include a leader sequence such as that found in the expression unit of extensin or tobacco PR-S.
  • a gene that encodes a protein that becomes sequestered in the cell wall, and which protein includes a unique epitope is considered to be particularly advantageous.
  • a secreted antigen marker would ideally employ an epitope sequence that would provide low background in plant tissue, a promoter-leader sequence that would impart efficient expression and targeting across the plasma membrane, and would produce protein that is bound in the cell wall and yet accessible to antibodies.
  • a normally secreted wall protein modified to include a unique epitope would satisfy all such requirements.
  • neo Paneo (Potrykus et al, 1985), which provides kanamycin resistance and can be selected for using kanamycin, G418, paromomycin, etc.; bar, which confers bialaphos or phosphinothricin resistance; a mutant EPSP synthase protein (Hinchee et al, 1988) conferring glyphosate resistance; a nitrilase such as bxn from Klebsiella ozaenae which confers resistance to bromoxynil (Stalker et al, 1988); a mutant acetolactate synthase (ALS) which confers resistance to imidazolinone, sulfonylurea or other ALS inhibiting chemicals (European Patent Application 154,204, 1985); a methotrexate resistant DHFR (Thillet et al, 1988), a dalapon dehalogenase
  • selectable marker capable of being used in systems to select transformants are those that encode the enzyme phosphinothricin acetyltransferase, such as the bar gene from Streptomyces hygroscopicus or the pat gene from Streptomyces viridochromogenes.
  • the enzyme phosphinothricin acetyl transferase (PAT) inactivates the active ingredient in the herbicide bialaphos, phosphinothricin (PPT). PPT inhibits glutamine synthetase, (Murakami et al, 1986; Twell et al, 1989) causing rapid accumulation of ammonia and cell death.
  • Screenable markers that may be employed include a ⁇ -glucuronidase (GUS) or uidA gene which encodes an enzyme for which various chromogenic substrates are known; an R-locus gene, which encodes a product that regulates the production of anthocyanin pigments (red color) in plant tissues (Dellaporta et al, 1988); a ⁇ -lactamase gene (Sutcliffe, 1978), which encodes an enzyme for which various chromogenic substrates are known (e.g., PAD AC, a chromogenic cephalosporin); a xylE gene (Zukowsky et al, 1983) which encodes a catechol dioxygenase that can convert chromogenic catechols; an ⁇ -amylase gene (JJkuta et al, 1990); a tyrosinase gene (Katz et al, 1983) which encodes an enzyme capable of oxidizing tyrosine to DOPA and
  • Another screenable marker contemplated for use in the present invention is firefly luciferase, encoded by the lux gene.
  • the presence of the lux gene in transformed cells may be detected using, for example, X-ray film, scintillation counting, fluorescent spectrophotometry, low-light video cameras, photon counting cameras or multiwell luminometry. It also is envisioned that this system may be developed for populational screening for bioluminescence, such as on tissue culture plates, or even for whole plant screening.
  • green fluorescent protein (GFP) is also contemplated as a particularly useful reporter gene (Sheen et al, 1995; Haseloff et al, 1997; Reichel et al, 1996; Tian et al, 1997; WO 97/41228). Expression of green fluorescent protein may be visualized in a cell or plant as fluorescence following illumination by particular wavelengths of light.
  • Antisense treatments represent one way of altering CT biosynthesis in accordance with the invention.
  • constructs comprising a CT biosynthesis gene and/or a promoter thereof in antisense orientation may be used to decrease or effectively eliminate the expression of CT in a plant. Accordingly, this may be used to increase anthocyanin accumulation in a plant or given plant tissue.
  • a Medicago truncatula or Arabidopsis thaliana BAN coding sequence could be used in this capacity, i this manner, the accumulation of CT precursors, including anthocyanins, could also be achieved.
  • antisense technology may be used to "knock-out" the function of a CT biosynthesis gene or homologous sequences thereof.
  • Antisense methodology takes advantage of the fact that nucleic acids tend to pair with "complementary" sequences.
  • complementary it is meant that polynucleotides are those which are capable of base-pairing according to the standard Watson-Crick complementarity rules. That is, the larger purines will base pair with the smaller pyrimidines to form combinations of guanine paired with cytosine (G:C) and adenine paired with either thymine (A:T) in the case of DNA, or adenine paired with uracil (A:U) in the case of RNA. Inclusion of less common bases such as inosine, 5-methylcytosine, 6-methyladenine, hypoxanthine and others in hybridizing sequences does not interfere with pairing.
  • Antisense polynucleotides when introduced into a target cell, specifically bind to their target polynucleotide and interfere with transcription, RNA processing, transport, translation and/or stability.
  • Antisense RNA constructs, or DNA encoding such antisense RNA's may be employed to inhibit gene transcription or translation or both within a host cell, either in vitro or in vivo, such as within a host animal, including a human subject.
  • Antisense constructs may be designed to bind to the promoter and other control regions, exons, infrons or even exon-intron boundaries of a gene. It is contemplated that the most effective antisense constructs will include regions complementary to intron/exon splice junctions. Thus, it is proposed that a preferred embodiment includes an antisense construct with complementarity to regions within 50-200 bases of an intron-exon splice junction. It has been observed that some exon sequences can be included in the construct without seriously affecting the target selectivity thereof. The amount of exonic material included will vary depending on the particular exon and intron sequences used. One can readily test whether too much exon DNA is included simply by testing the constructs in vitro to determine whether normal cellular function is affected or whether the expression of related genes having complementary sequences is affected.
  • complementary or “antisense” means polynucleotide sequences that are substantially complementary over their entire length and have very few base mismatches. For example, sequences of fifteen bases in length may be termed complementary when they have complementary nucleotides at thirteen or fourteen positions. Naturally, sequences which are completely complementary will be sequences which are entirely complementary throughout their entire length and have no base mismatches. Other sequences with lower degrees of homology also are contemplated. For example, an antisense construct which has limited regions of high homology, but also contains a non-homologous region (e.g., ribozyme; see above) could be designed. These molecules, though having less than 50% homology, would bind to target sequences under appropriate conditions.
  • genomic DNA may be combined with cDNA or synthetic sequences to generate specific constructs.
  • a genomic clone will need to be used.
  • the cDNA or a synthesized polynucleotide may provide more convenient restriction sites for the remaining portion of the construct and, therefore, would be used for the rest of the sequence.
  • Tissue cultures may be used in certain transformation techniques for the preparation of cells for transformation and for the regeneration of plants therefrom. Maintenance of tissue cultures requires use of media and controlled environments. "Media” refers to the numerous nutrient mixtures that are used to grow cells in vitro, that is, outside of the intact living organism. The medium usually is a suspension of various categories of ingredients (salts, amino acids, growth regulators, sugars, buffers) that are required for growth of most cell types. However, each specific cell type requires a specific range of ingredient proportions for growth, and an even more specific range of formulas for optimum growth. Rate of cell growth also will vary among cultures initiated with the array of media that permit growth of that cell type.
  • Nutrient media is prepared as a liquid, but this may be solidified by adding the liquid to materials capable of providing a solid support.
  • Agar is most commonly used for this purpose.
  • Bactoagar, Hazelton agar, Gelrite, and Gelgro are specific types of solid support that are suitable for growth of plant cells in tissue culture.
  • Some cell types will grow and divide either in liquid suspension or on solid media. As disclosed herein, plant cells will grow in suspension or on solid medium, but regeneration of plants from suspension cultures typically requires transfer from liquid to solid media at some point in development. The type and extent of differentiation of cells in culture will be affected not only by the type of media used and by the environment, for example, pH, but also by whether media is solid or liquid.
  • Tissue that can be grown in a culture includes meristem cells, Type I, Type JJ, and Type III callus, immature embryos and gametic cells such as microspores, pollen, sperm and egg cells.
  • Type I, Type II, and Type III callus may be initiated from tissue sources including, but not limited to, immature embryos, seedling apical meristems, root, leaf, microspores and the like. Those cells which are capable of proliferating as callus also are recipient cells for genetic transformation.
  • Somatic cells are of various types. Embryogenic cells are one example of somatic cells which may be induced to regenerate a plant through embryo formation. Non-embryo genie cells are those which typically will not respond in such a fashion. Certain techniques may be used that enrich recipient cells within a cell population. For example, Type II callus development, followed by manual selection and culture of friable, embryogenic tissue, generally results in an enrichment of cells. Manual selection techniques which can be employed to select target cells may include, e.g., assessing cell morphology and differentiation, or may use various physical or biological means. Cryopreservation also is a possible method of selecting for recipient cells.
  • Manual selection of recipient cells is one means that may be used in an attempt to enrich for particular cells prior to culturing (whether cultured on solid media or in suspension).
  • cultured cells may be grown either on solid supports or in the form of liquid suspensions, hi either instance, nutrients may be provided to the cells in the form of media, and environmental conditions controlled.
  • tissue culture media comprised of various amino acids, salts, sugars, growth regulators and vitamins. Most of the media employed in the practice of the invention will have some similar components, but may differ in the composition and proportions of their ingredients depending on the particular application envisioned.
  • Suitable methods for transformation of plant or other cells for use with the current invention are believed to include virtually any method by which DNA can be introduced into a cell, such as by direct delivery of DNA such as by PEG-mediated transformation of protoplasts (Omirulleh et al, 1993), by desiccation/inhibition-mediated DNA uptake (Potrykus et al, 1985), by electroporation (U.S. Patent No. 5,384,253, specifically incorporated herein by reference in its entirety), by agitation with silicon carbide fibers (Kaeppler et al, 1990; U.S. Patent No. 5,302,523, specifically inco ⁇ orated herein by reference in its entirety; and U.S. Patent No.
  • Agrobacterium-mediated transfer is a widely applicable system for introducing genes into plant cells because the DNA can be introduced into whole plant tissues, thereby bypassing the need for regeneration of an intact plant from a protoplast.
  • the use of Agrobacterium-mediated plant integrating vectors to introduce DNA into plant cells is well known in the art. See, for example, the methods described by Fraley et ⁇ l, (1985), Rogers et ⁇ l, (1987) and U.S. Patent No. 5,563,055, specifically inco ⁇ orated herein by reference in its entirety.
  • Agrobacterium-mediated transformation is most efficient in dicotyledonous plants and is the preferable method for transformation of dicots, including Arabidopsis, tobacco, tomato, alfalfa and potato. Indeed, while Agrobacterium-mediated transformation has been routinely used with dicotyledonous plants for a number of years, it has only recently become applicable to monocotyledonous plants. Advances in Agrobacterium-mediated transformation techniques have now made the technique applicable to nearly all monocotyledonous plants. For example, Agrobacterium-mediated transformation techniques have now been applied to rice (Hiei et ⁇ l., 1997; U.S. Patent No.
  • friable tissues such as a suspension culture of cells or embryogenic callus or alternatively one may transform immature embryos or other organized tissue directly.
  • pectolyases pectolyases
  • mechanically wounding in a controlled manner.
  • some species which have been transformed by electroporation of intact cells include maize (U.S. Patent No.
  • One also may employ protoplasts for electroporation transformation of plants (Bates, 1994; Lazzeri, 1995).
  • protoplasts for electroporation transformation of plants
  • the generation of transgenic soybean plants by electroporation of cotyledon-derived protoplasts is described by Dhir and Widholm in Intl. Patent Appl. Publ. No. WO 9217598 (specifically inco ⁇ orated herein by reference).
  • Other examples of species for which protoplast transformation has been described include barley (Lazerri, 1995), sorghum (Battraw et ⁇ l, 1991), maize (Bhattacharjee et ⁇ l, 1997), wheat (He et ⁇ l, 1994) and tomato (Tsukada, 1989).
  • microprojectile bombardment U.S. Patent No. 5,550,318; U.S. Patent No.
  • particles may be coated with nucleic acids and delivered into cells by a propelling force.
  • Exemplary particles include those comprised of tungsten, platinum, and preferably, gold. It is contemplated that in some instances DNA precipitation onto metal particles would not be necessary for DNA delivery to a recipient cell using microprojectile bombardment. However, it is contemplated that particles may contain DNA rather than be coated with DNA. Hence, it is proposed that DNA-coated particles may increase the level of DNA delivery via particle bombardment but are not, in and of themselves, necessary.
  • cells in suspension are concentrated on filters or solid culture medium.
  • immature embryos or other target cells may be arranged on solid culture medium.
  • the cells to be bombarded are positioned at an appropriate distance below the macroprojectile stopping plate.
  • An illustrative embodiment of a method for delivering DNA into plant cells by acceleration is the Biolistics Particle Delivery System, which can be used to propel particles coated with DNA or cells through a screen, such as a stainless steel or Nytex screen, onto a filter surface covered with monocot plant cells cultured in suspension. The screen disperses the particles so that they are not delivered to the recipient cells in large aggregates.
  • Microprojectile bombardment techniques are widely applicable, and may be used to transform virtually any plant species. Examples of species for which have been transformed by microprojectile bombardment include monocot species such as maize (PCT Application WO 95/06128), barley (Ritala et al, 1994; Hensgens et al, 1993), wheat (U.S. Patent No.
  • Transformation of protoplasts can be achieved using methods based on calcium phosphate precipitation, polyethylene glycol treatment, electroporation, and combinations of these treatments (see, e.g., Potrykus et al, 1985; Lorz et al, 1985; Omirulleh et al, 1993; Fromm et al, 1986; Uchimiya et al, 1986; Callis et al, 1987; Marcotte et al, 1988).
  • Examples of the use of direct uptake transformation of cereal protoplasts include transformation of rice (Ghosh-Biswas et al, 1994), sorghum (Battraw and Hall, 1991), barley (Lazerri, 1995), oat (Zheng and Edwards, 1990) and maize (Omirulleh et al, 1993).
  • the next steps generally concern identifying the transformed cells for further culturing and plant regeneration.
  • identifying the transformed cells for further culturing and plant regeneration.
  • one may desire to employ a selectable or screenable marker gene with a transformation vector prepared in accordance with the invention.
  • DNA is introduced into only a small percentage of target cells in any one experiment.
  • a means for selecting those cells that are stably transformed is to introduce into the host cell, a marker gene which confers resistance to some normally inhibitory agent, such as an antibiotic or herbicide.
  • antibiotics which may be used include the aminoglycoside antibiotics neomycin, kanamycin and paromomycin, or the antibiotic hygromycin.
  • aminoglycoside antibiotics Resistance to the aminoglycoside antibiotics is conferred by aminoglycoside phosphostransferase enzymes such as neomycin phosphotransferase II (NPT II) or NPT I, whereas resistance to hygromycin is conferred by hygromycin phosphotransferase.
  • aminoglycoside phosphostransferase enzymes such as neomycin phosphotransferase II (NPT II) or NPT I
  • hygromycin phosphotransferase Resistance to the aminoglycoside antibiotics is conferred by aminoglycoside phosphostransferase enzymes such as neomycin phosphotransferase II (NPT II) or NPT I
  • NPT II neomycin phosphotransferase II
  • hygromycin phosphotransferase Resistance to the aminoglycoside antibiotics is conferred by aminoglycoside phosphostransferase
  • surviving cells are those cells where, generally, the resistance-conferring gene has been integrated and expressed at sufficient levels to permit cell survival. Cells may be tested further to confirm stable integration of the exogenous DNA.
  • Bialaphos is a tripeptide antibiotic produced by Streptomyces hygroscopicus and is composed of phosphinothricin (PPT), an analogue of L-glutamic acid, and two L-alanine residues. Upon removal of the L-alanine residues by intracellular peptidases, the PPT is released and is a potent inhibitor of glutamine synthetase (GS), a pivotal enzyme involved in ammonia assimilation and nitrogen metabolism (Ogawa et al, 1973). Synthetic PPT, the active ingredient in the herbicide LibertyTM also is effective as a selection agent. Inhibition of GS in plants by PPT causes the rapid accumulation of ammonia and death of the plant cells.
  • the organism producing bialaphos and other species of the genus Streptomyces also synthesizes an enzyme phosphinothricin acetyl transferase (PAT) which is encoded by the bar gene in Streptomyces hygroscopicus and the pat gene in Streptomyces viridochromogenes.
  • PAT phosphinothricin acetyl transferase
  • the use of the herbicide resistance gene encoding phosphinothricin acetyl transferase (PAT) is referred to in DE 3642 829 A, wherein the gene is isolated from Streptomyces viridochromogenes.
  • this enzyme acetylates the free amino group of PPT preventing auto-toxicity (Thompson et al, 1987).
  • the bar gene has been cloned (Murakami et al, 1986; Thompson et al, 1987) and expressed in transgenic tobacco, tomato, potato (De Block et al, 1987) Brassica (De Block et al, 1989) and maize (U.S. Patent No. 5,550,318).
  • some transgenic plants which expressed the resistance gene were completely resistant to commercial formulations of PPT and bialaphos in greenhouses.
  • Another example of a herbicide which is useful for selection of transformed cell lines in the practice of the invention is the broad spectrum herbicide glyphosate.
  • Glyphosate inhibits the action of the enzyme EPSPS which is active in the aromatic amino acid biosynthetic pathway. Inhibition of this enzyme leads to starvation for the amino acids phenylalanine, tyrosine, and tryptophan and secondary metabolites derived thereof.
  • U.S. Patent No. 4,535,060 describes the isolation of EPSPS mutations which confer glyphosate resistance on the Salmonella typhimurium gene for EPSPS, aroA. The EPSPS gene was cloned from Zea mays and mutations similar to those found in a glyphosate resistant aroA gene were introduced in vitro.
  • Mutant genes encoding glyphosate resistant EPSPS enzymes are described in, for example, International Patent WO 97/4103.
  • the best characterized mutant EPSPS gene conferring glyphosate resistance comprises amino acid changes at residues 102 and 106, although it is anticipated that other mutations will also be useful (PCT/WO97/4103).
  • transformed tissue is cultured for 0 - 28 days on nonselective medium and subsequently transferred to medium containing from 1-3 mg/1 bialaphos or 1-3 mM glyphosate as appropriate. While ranges of 1-3 mg/1 bialaphos or 1-3 mM glyphosate will typically be preferred, it is proposed that ranges of
  • the herbicide DALAPON 2,2-dichloropropionic acid
  • the enzyme 2,2-dichloropropionic acid dehalogenase inactivates the herbicidal activity of 2,2-dichloropropionic acid and therefore confers herbicidal resistance on cells or plants expressing a gene encoding the dehalogenase enzyme (Buchanan-Wollaston et al, 1992; U.S. Patent No. 5,508,468; and U.S. Patent No. 5,508,468; each of the disclosures of which is specifically inco ⁇ orated herein by reference in its entirety).
  • anthranilate synthase which confers resistance to certain amino acid analogs, e.g., 5-methyltryptophan or 6-methyl anthranilate, may be useful as a selectable marker gene.
  • an anthranilate synthase gene as a selectable marker was described in U.S. Patent No. 5,508,468.
  • a screenable marker trait is the enzyme luciferase.
  • cells expressing luciferase emit light which can be detected on photographic or x-ray film, in a luminometer (or liquid scintillation counter), by devices that enhance night vision, or by a highly light sensitive video camera, such as a photon counting camera.
  • luciferase enzyme luciferase
  • a highly light sensitive video camera such as a photon counting camera.
  • the photon counting camera is especially valuable as it allows one to identify specific cells or groups of cells which are expressing luciferase and manipulate those in real time.
  • Another screenable marker which may be used in a similar fashion is the gene coding for green fluorescent protein.
  • a selection agent such as bialaphos or glyphosate
  • selection with a growth inhibiting compound, such as bialaphos or glyphosate at concentrations below those that cause 100% inhibition followed by screening of growing tissue for expression of a screenable marker gene such as luciferase would allow one to recover transformants from cell or tissue types that are not amenable to selection alone.
  • combinations of selection and screening may enable one to identify transformants in a wider variety of cell and tissue types. This may be efficiently achieved using a gene fusion between a selectable marker gene and a screenable marker gene, for example, between an NPTII gene and a GFP gene.
  • Cells that survive the exposure to the selective agent, or cells that have been scored positive in a screening assay, may be cultured in media that supports regeneration of plants.
  • MS and N6 media may be modified by including further substances such as growth regulators.
  • growth regulators is dicamba or 2,4-D.
  • other growth regulators may be employed, including NAA, NAA + 2,4-D or picloram.
  • Media improvement in these and like ways has been found to facilitate the growth of cells at specific developmental stages. Tissue may be maintained on a basic media with growth regulators until sufficient tissue is available to begin plant regeneration efforts, or following repeated rounds of manual selection, until the mo ⁇ hology of the tissue is suitable for regeneration, at least 2 wk, then transferred to media conducive to maturation of embryoids.
  • Cultures are transferred every 2 wk on this medium.
  • Shoot development will signal the time to transfer to medium lacking growth regulators.
  • the transformed cells identified by selection or screening and cultured in an appropriate medium that supports regeneration, will then be allowed to mature into plants.
  • Developing plantlets are transferred to soiless plant growth mix, and hardened, e.g., in an environmentally controlled chamber, for example, at about 85% relative humidity, 600 ppm CO 2 , and 25-250 microeinsteins m "2 s "1 of light.
  • Plants are preferably matured either in a growth chamber or greenhouse. Plants can be regenerated from about 6 wk to 10 months after a transformant is identified, depending on the initial tissue.
  • cells are grown on solid media in tissue culture vessels. Illustrative embodiments of such vessels are petri dishes and Plant Cons.
  • Regenerating plants are preferably grown at about 19 to 28°C. After the regenerating plants have reached the stage of shoot and root development, they may be transferred to a greenhouse for further growth and testing.
  • Seeds on transformed plants may occasionally require embryo rescue due to cessation of seed development and premature senescence of plants.
  • To rescue developing embryos they are excised from surface-disinfected seeds 10-20 days post-pollination and cultured.
  • An embodiment of media used for culture at this stage comprises MS salts, 2% sucrose, and 5.5 g/1 agarose.
  • embryo rescue large embryos (defined as greater than 3 mm in length) are germinated directly on an appropriate media. Embryos smaller than that may be cultured for 1 wk on media containing the above ingredients along with 10 "5 M abscisic acid and then transferred to growth regulator-free medium for germination.
  • assays include, for example, “molecular biological” assays, such as Southern and Northern blotting and PCRTM; “biochemical” assays, such as detecting the presence of a protein product, e.g., by immunological means (ELISAs and Western blots) or by enzymatic function; plant part assays, such as leaf or root assays; and also, by analyzing the phenotype of the whole regenerated plant.
  • Genomic DNA may be isolated from cell lines or any plant parts to determine the presence of the exogenous gene through the use of techniques well known to those skilled in the art. Note, that intact sequences will not always be present, presumably due to rearrangement or deletion of sequences in the cell.
  • the presence of DNA elements introduced through the methods of this invention may be determined, for example, by polymerase chain reaction (PCRTM). Using this technique, discreet fragments of DNA are amplified and detected by gel electrophoresis. This type of analysis permits one to determine whether a gene is present in a stable transformant, but does not prove integration of the introduced gene into the host cell genome. It is typically the case, however, that DNA has been integrated into the genome of all transformants that demonstrate the presence of the gene through PCRTM analysis.
  • PCRTM polymerase chain reaction
  • PCRTM techniques it is not typically possible using PCRTM techniques to determine whether transformants have exogenous genes introduced into different sites in the genome, i.e., whether transformants are of independent origin. It is contemplated that using PCRTM techniques it would be possible to clone fragments of the host genomic DNA adjacent to an introduced gene.
  • Positive proof of DNA integration into the host genome and the independent identities of transformants may be determined using the technique of Southern hybridization. Using this technique specific DNA sequences that were introduced into the host genome and flanking host ⁇ DNA sequences can be identified. Hence the Southern hybridization pattern of a given transformant serves as an identifying characteristic of that transformant. In addition it is possible through Southern hybridization to demonstrate the presence of introduced genes in high molecular weight DNA, i.e., confirm that the introduced gene has been integrated into the host cell genome.
  • the technique of Southern hybridization provides information that is obtained using PCRTM, e.g., the presence of a gene, but also demonstrates integration into the genome and characterizes each individual transformant.
  • RNA will only be expressed in particular cells or tissue types and hence it will be necessary to prepare RNA for analysis from these tissues.
  • PCRTM techniques also may be used for detection and quantitation of RNA produced from introduced genes.
  • PCRTM it is first necessary to reverse transcribe RNA into DNA, using enzymes such as reverse transcriptase, and then through the use of conventional PCRTM techniques amplify the DNA. In most instances PCRTM techniques, while useful, will not demonstrate integrity of the RNA product. Further information about the nature of the RNA product may be obtained by Northern blotting. This technique will demonstrate the presence of an RNA species and give information about the integrity of that RNA. The presence or absence of an RNA species also can be detennined using dot or slot blot Northern hybridizations. These techniques are modifications of Northern blotting and will only demonstrate the presence or absence of an RNA species.
  • Southern blotting and PCRTM may be used to detect the gene(s) in question, they do not provide information as to whether the corresponding protein is being expressed. Expression may be evaluated by specifically identifying the protein products of the introduced genes or evaluating the phenotypic changes brought about by their expression.
  • Assays for the production and identification of specific proteins may make use of physical-chemical, structural, functional, or other properties of the proteins.
  • Unique physical- chemical or structural properties allow the proteins to be separated and identified by electrophoretic procedures, such as native or denaturing gel electrophoresis or isoelectric focusing, or by chromatographic techniques such as ion exchange or gel exclusion chromatography.
  • the unique structures of individual proteins offer opportunities for use of specific antibodies to detect their presence in formats such as an ELISA assay. Combinations of approaches may be employed with even greater specificity such as western blotting in which antibodies are used to locate individual gene products that have been separated by electrophoretic techniques. Additional techniques may be employed to absolutely confirm the identity of the product of interest such as evaluation by amino acid sequencing following purification. Although these are among the most commonly employed, other procedures may be additionally used.
  • Assay procedures also may be used to identify the expression of proteins by their functionality, especially the ability of enzymes to catalyze specific chemical reactions involving specific substrates and products. These reactions may be followed by providing and quantifying the loss of substrates or the generation of products of the reactions by physical or chemical procedures. Examples are as varied as the enzyme to be analyzed and may include assays for PAT enzymatic activity by following production of radiolabeled acetylated phosphinothricin from phosphinothricin and ,4 C-acetyl CoA or for anthranilate synthase activity by following loss of fluorescence of anthranilate, to name two.
  • Bioassays Very frequently the expression of a gene product is determined by evaluating the phenotypic results of its expression. These assays also may take many forms including but not limited to analyzing changes in the chemical composition, mo ⁇ hology, or physiological properties of the plant. Chemical composition may be altered by expression of genes encoding enzymes or storage proteins which change amino acid composition and may be detected by amino acid analysis, or by enzymes which change starch quantity which may be analyzed by near infrared reflectance spectrometry. Mo ⁇ hological changes may include greater stature or tliicker stalks. Most often changes in response of plants or plant parts to imposed treatments are evaluated under carefully controlled conditions termed bioassays.
  • transgenic plants may be made by crossing a plant having a selected DNA of the invention to a second plant lacking the construct.
  • a selected CT biosynthesis gene can be introduced into a particular plant variety by crossing, without the need for ever directly transforming a plant of that given variety. Therefore, the current invention not only encompasses a plant directly transformed or regenerated from cells which have been fransformed in accordance with the current invention, but also the progeny of such plants.
  • progeny denotes the offspring of any generation of a parent plant prepared in accordance with the instant invention, wherein the progeny comprises a selected DNA construct prepared in accordance with the invention.
  • Crossing a plant to provide a plant line having one or more added transgenes relative to a starting plant line, as disclosed herein, is defined as the techniques that result in a transgene of the invention being introduced into a plant line by crossing a starting line with a donor plant line that comprises a transgene of the invention. To achieve this one could, for example, perform the following steps:
  • step (d) repeating steps (b) and (c) for the pu ⁇ ose of transferring a desired DNA sequence from a plant of a first genotype to a plant of a second genotype.
  • Introgression of a DNA element into a plant genotype is defined as the result of the process of backcross conversion.
  • a plant genotype into which a DNA sequence has been introgressed may be referred to as a backcross converted genotype, line, inbred, or hybrid.
  • a plant genotype lacking the desired DNA sequence may be referred to as an unconverted genotype, line, inbred, or hybrid.
  • Condensed tannin (CT) biosynthesis gene A gene encoding a polypeptide that catalyzes one or more steps in the biosynthesis of condensed tannins.
  • Expression The combination of intracellular processes, including transcription and translation undergone by a coding DNA molecule such as a structural gene to produce a polypeptide.
  • Genetic Transformation A process of introducing a DNA sequence or construct (e.g., a vector or expression cassette) into a cell or protoplast in which that exogenous DNA is inco ⁇ orated into a chromosome or is capable of autonomous replication.
  • a DNA sequence or construct e.g., a vector or expression cassette
  • Heterologous A sequence which is not normally present in a given host genome in the genetic context in which the sequence is currently found In this respect, the sequence may be native to the host genome, but be rearranged with respect to other genetic sequences within the host sequence.
  • a regulatory sequence may be heterologous in that it is linked to a different coding sequence relative to the native regulatory sequence.
  • obtaining When used in conjunction with a transgenic plant cell or transgenic plant, obtaining means either transforming a non-transgenic plant cell or plant to create the transgenic plant cell or plant, or planting transgenic plant seed to produce the transgenic plant cell or plant.
  • a transgenic plant seed may be from an R 0 transgenic plant or may be from a progeny of any generation thereof that inherits a given transgenic sequence from a starting transgenic parent plant.
  • Promoter A recognition site on a DNA sequence or group of DNA sequences that provides an expression control element for a structural gene and to which RNA polymerase specifically binds and initiates RNA synthesis (transcription) of that gene.
  • Ro transgenic plant A plant that has been genetically transformed or has been regenerated from a plant cell or cells that have been genetically fransformed.
  • Regeneration The process of growing a plant from a plant cell (e.g., plant protoplast, callus or explant).
  • Selected DNA A DNA segment which one desires to introduce into a plant genome by genetic transformation.
  • Transformation construct A chimeric DNA molecule which is designed for introduction into a host genome by genetic fransformation.
  • Preferred transformation constructs will comprise all of the genetic elements necessary to direct the expression of one or more exogenous genes.
  • Transformed cell A cell the DNA complement of which has been altered by the introduction of an exogenous DNA molecule into that cell.
  • Transgene A segment of DNA which has been inco ⁇ orated into a host genome or is capable of autonomous replication in a host cell and is capable of causing the expression of one or more coding sequences. Exemplary transgenes will provide the host cell, or plants regenerated therefrom, with a novel phenotype relative to the corresponding non-transformed cell or plant. Transgenes may be directly introduced into a plant by genetic transformation, or may be inherited from a plant of any previous generation which was transformed with the DNA segment.
  • Transgenic plant A plant or progeny plant of any subsequent generation derived therefrom, wherein the DNA of the plant or progeny thereof contains an introduced exogenous DNA segment not naturally present in a non-transgenic plant of the same strain.
  • the transgenic plant may additionally contain sequences which are native to the plant being transformed, but wherein the "exogenous" gene has been altered in order to alter the level or pattern of expression of the gene, for example, by use of one or more heterologous regulatory or other elements.
  • a plasmid is an exemplary vector. IX. Examples
  • RNA isolated from the first three to four newly emerged siliques was used to synthesize first strand cDNA in a volume of 20 ⁇ l containing 20 mM Tris-HCl pH 8.4, 50 mM KC1 2 , 5 mM MgCl 2 , 10 mM DDT, 1 mM deoxyribonucleotide triphosphate mixture, 500 ng oligo (dT)12-18 (GibcoBRL), 25 units of RNA Out (Gibco BRL) and 200 units of Moloney murine leukemia virus reverse transcriptase SuperScriptll (Gibco BRL) for 60 min at 42°C.
  • Coding regions for expression in plants were first cloned into the pRTL2 vector.
  • Gene constructs carrying a double cauliflower mosaic virus 35S promoter:: gene coding region: :35S poly (A) transcription termination region were cut from the pRTL2 plasmid and cloned into pCAMBIA2300 and pCAMBIA3300 binary vectors for plant transformation.
  • Arabidopsis transformants were prepared using the floral dip method (Clough and Bent, 1999). The primary transgenic plants were initially screened by RT-PCR by using Ready-To-Go PCR beads (Pharmacia). The basic recombinant DNA techniques used in the gene cloning were as described by Sambrook et al. (1989). Forty BAN transgenic Col-0 Arabidopsis plants were analyzed using RT-PCR. RNA was first isolated from leaf tissues harvested from greenhouse grown plants using RNAzol.
  • the BAN and actin gene-specific primers (actin: forward primer, GATATGGAAAAGATCTGGCATCAC (SEQ ID NO:9); reverse primer, TCATACTCGGCCTTGGAGATCCAC (SEQ JD NO: 10) were used to monitor the BAN mRNA expression level in comparison to that of the constitutive actin control.
  • actin forward primer, GATATGGAAAAGATCTGGCATCAC (SEQ ID NO:9)
  • reverse primer TCATACTCGGCCTTGGAGATCCAC (SEQ JD NO: 10
  • CTs in leaves or seeds were extracted in 70% aqueous acetone containing 5.26 mM sodium metabisulphite as the antioxidant. The extracts were directly analyzed by the butanol /HCI reaction. Five ml of butanol/HCL mixture (95% butan-1- ol and 5% concentrated HCI) was added to 1ml of sample in polypropylene tubes. The tubes were heated in a water bath at 95°C for 1 hr, cooled and read at 550 nm on a spectrophotometer. Unheated blanks were prepared in an identical manner and measured to correct for the background absorbance of the sample.
  • Extracts from seeds and leaves o ⁇ Arabidopsis plants expressing the BAN gene contained a strong peak at a retention time (RT) of approximately 22.9 min, the only major peak between 10 and 30 min RT. This peak was also present at high levels in Col-0 Arabidopsis seeds, but was completely absent from leaves of Col-0 or ban Arabidopsis. The nature of this compound is yet to be determined. Its levels are expressed as mg catechin equivalents in Table 2.
  • Example 2 Expression of the BAN gene reduces anthocyanin levels in the PAP-ID mutant of Arabidopsis
  • the PAP-1 gene of Arabidopsis encodes a MYB transcription factor (Borevitz et al, 2000). Over-expression of PAP-1 leads to strong constitutive induction of the complete pathway leading to anthocyanins in Arabidopsis.
  • the pap-ID mutant of Arabidopsis over-expresses PAP-1 by virtue of the insertion of a T-DNA activation tag close to the 5 '-end of the PAP-1 gene, and ectopically accumulates anthocyanins throughout the plant, resulting in a strong pu ⁇ le coloration (Borevitz et al, 2000).
  • the PAPl-D mutant was transformed with Agrobacterium harboring the full length Arabidopsis ban cDNA under control of a double 35S promoter (p2xS35 ::i 4N) using the floral dip method (Clough and Bent, 1999). Most of the 2xS35: :BAN transformed PAPl-D plants lost the pu ⁇ le anthocyanin pigmentation in their leaves. Some of these plants were analyzed for expression o ⁇ PAP, BAN and actin genes by RT-PCR.
  • PAPl-D primers used for RT-PCR were: forward primer, GGATCCATGGAGGGTTCGTCCAAAGGGCTGCG (SEQ JD NO: 11) and reverse primer, TCTAGACTCGAGATCAAATTTCACAGTCTCTCC (SEQ ID NO: 12).
  • the BAN gene product acts on leucoanthocyanidin, a substrate common for both CT and anthocyanin biosynthesis, diverting it into the CT pathway.
  • BAN would be a leucoanthocyanidin reductase that had a higher affinity for leucoanthocyanidin or a higher activity in the fransformed tissues than leucoanthocyanidin dioxygenase (anthocyanidin synthase), the enzyme that channels leucoanthocyanidin into the anthocyanin pathway (Saito et al, 1999).
  • Example 3 Cloning of a BAN gene from the forage legume Medicago truncatula
  • Unvernalized seeds o ⁇ Medicago truncatula cv Jemalong line A-17 were planted in pots and seedlings grown in the greenhouse. After pollination of flowers, young seed pods were collected and young seeds about 2-5 mm in size were removed from the pods, dropped in liquid nitrogen, and stored at -80°C.
  • Total RNA was extracted from young seeds using a Qiagen Midi kit RNA isolation kit, and mRNA obtained from the total RNA using a poly(A) mRNA purification kit (Qiagen).
  • a cDNA library was constructed from the mRNA using a Stratagene ZAP-cDNA synthesis kit and ZAP-cDNA Gigapack III Gold cloning kit, according to the manufacturer's protocols.
  • Mass excision of the cDNA library was performed using 1 ⁇ l primary cDNA library (about 10, 000 pfu of phage) following the protocol of the Stratagene kit.
  • One ⁇ l of mass excised plasmids was used for plating with E. coli SoLR cells following the protocols in the Stratagene kit.
  • Five thousand colonies were picked individually and each incubated in 1.5ml TB medium with 100 ⁇ g/ml ampicillin contained in wells of 96-well plates.
  • Plasmids were prepared and inserts sequenced following a robotic plasmid preparation/sequencing protocol utilizing a crude alkaline lysis technique for plasmid isolation (Roe, 1996) followed by automated sequencing with an ABI 3700 capillary sequencer and Big Dye terminator chemistry.
  • genomic DNA was extracted from M. truncatula leaves. Ten ⁇ g of DNA was digested with the restriction enzymes Hz ' ndLU and EcoRI at 37°C overnight, and fragments resolved by electrophoresis in a 0.8% agarose gel with Tris-acetic acid- ⁇ DTA (TA ⁇ ) buffer. The complete M. truncatula putative BAN open reading frame was labeled with 32 P-dCTP using a random primer labeling kit from Promega (Prime-a-Gene ® labeling system) and used as probe. DNA gel blot hybridization was performed according to standard protocols (Sambrook et al, 1989; Church and Gilbert, 1984). The results indicated the presence of a single copy of the putative BAN gene in the M. truncatula genome.
  • hypocotyls were collected from seedlings either grown in the dark to suppress anthocyanin accumulation or grown under high light to induce anthocyanin accumulation. Seeds were scarified with concentrated sulfuric acid for 10 min and then washed several times with sterile MilliQ water, before placing on wet Whatman 3M paper in clear petri dishes for germination in the dark. White hypocotyls were harvested from five-day old dark grown plants.
  • RNA preparation solution 0.5X formaldehyde gel-running buffer, 2.2 M formaldehyde, 50% formamide
  • RNA samples After centrifugation, 2 ⁇ l formaldehyde gel-loading buffer (50% glycerol, 1 mM EDTA pH 8.0, 0.25% bromophenol blue, 0.25% xylene cyanol FF) was added to RNA samples, which were then electrophoresed in 1.5% agarose gels in the presence of ethidium bromide (l ⁇ g/20 ⁇ l). RNAs were then transfer blotted to GeneScreen Plus ® (NEN/Dupont) membranes.
  • formaldehyde gel-loading buffer 50% glycerol, 1 mM EDTA pH 8.0, 0.25% bromophenol blue, 0.25% xylene cyanol FF
  • Membranes were pre-hybridized at 65°C in hybridization buffer (1% BSA, 1 mM EDTA pH 8.0, 0.5 M NaHPO 4 pH 7.2, 7% SDS) for 4 hours, then labeled probes were added to the hybridization solution and allowed to hybridize with the membrane overnight at 65°C.
  • the BAN gene coding region probe was labeled with ⁇ - 32 P dCTP using a Promega Prime-a-Gene ® labeling system random primer labeling kit.
  • Hybridized membranes were washed twice for 10 min in wash buffer #1 (0.5% BSA, 1 mM EDTA, 40 mM NaHPO 4 pH 7.2, 5% SDS), then twice for 5-10 min in wash buffer #2 (1 mM EDTA, 40 mM NaHPO 4 pH 7.2, 1% SDS). Membranes were then exposed overnight in a phosphorimager or exposed to X-ray film at -80°C for 48-72 hr. BAN RNA levels were also determined using an RT-PCR method. One ⁇ g total RNA sample was used for the first strand cDNA synthesis using an AdvantageTM RT-for-PCR kit (Clonetech).
  • PCR reactions Five ⁇ l of the first strand cDNA was used for each PCR reaction in 50 ⁇ l final volume.
  • the PCR reactions were done using M. truncatula BAN gene primers (forward 5'CCTCATAGCACTGCAAAGTTTGGGGG3' (SEQ ID NO:13) and reverse 5'GCCTGTTAG AAGTGACATTCCC3' (SEQ ID NO:14)).
  • the cycle conditions were 94°C for 2 min; 30 cycles at 94°C for 30 sec, 60°C for 30 sec and 72°C for 1.5 min, followed by a final extension at 72°C for 10 min.
  • Products of PCR amplification were analyzed by electrophoresis of 20 ⁇ l reaction aliquots on 0.8% agarose gels in Tris-acetic acid-EDTA buffer and visualized with ethidium bromide.
  • the binary vector pBI121-BAN was constructed by inserting the complete M. truncatula BAN open reading frame into the BamHI and S ⁇ cl sites of pBI121 (Clonetech). In this construct,
  • BAN expression is under control of the cauliflower mosaic virus 35S promoter and Nos 3' terminator.
  • pBI121-BAN was transformed into Agrobacterium tumefaciens LBA4404 by electroporation.
  • Leaves of tobacco (Nicotiana tabacum cv. Xanthi) seedlings were cut into discs about 1 cm 2 in size, and these were pre-cultured for 3 days on MS 104 medium consisting of MSO [containing 4.3 g/1 MS salts (Gibco) (Murashige and Skoog, 1962), 1 ml/1 B5 vitamins (Sigma) (Gamborg et al, 1968), 30g/l sucrose, and 0.3% (w/v) phytogel, pH 5.7], 1.0 mg/1 benzyladenine (BA) and 0.1 mg/1 naphthalene acetic acid (NAA). A single colony of A.
  • MS 104 medium consisting of MSO [containing 4.3 g/1 MS salts (Gibco) (Murashige and Skoog, 1962), 1 ml/1 B5 vitamins (Sigma) (Gamborg et al, 1968), 30g/l sucrose, and 0.3% (w/v) phytogel, pH 5.7],
  • tumefaciens harboring pBI121-BAN was grown overnight in the dark in Luria-Bertani medium (Sambrook et al, 1989) containing 100 mg/1 streptomycin (Sigma) and 50 mg/1 kanamycin (Sigma) at 28°C on a gyratory shaker set at 250 rpm. Bacteria from this culture were pelleted and then re-suspended in 50 ml sterile MSO liquid medium. The pre-cultured leaf discs were dipped into the bacterial suspension for 10 min, blotted dry on sterile Whatman paper, and inoculated on solid MS 104 medium for co-cultivation for 3 days.
  • the infected leaf discs were then further selected on MS 104 medium supplemented with 300 mg/1 kanamycin and 500 mg/1 carbenicillin.
  • Putative transgenic shoots were rooted on rooting medium consisting of MSO supplemented with 200 mg/1 kanamycin and 500 mg/1 carbenicillin. Thirty eight putative transgenic plantlets were transferred to pots and grown in the greenhouse.
  • genomic DNA was extracted from leaves of putative transgenic tobacco plants.
  • One hundred to 150 mg of fresh leaf tissue was processed using the DNeasy® Plant Minikit (Qiagen). After digestion with HindHI, eight ⁇ g of genomic DNA were separated by electrophoresis as described above.
  • the NPTII selectable marker gene in the binary vector was used as probe; it was labeled with 32 P-dCTP using the Ready-To-Go DNA labeling beads (dCTP) kit (Amersham Pharmacia Biotech).
  • Membranes were pre-hybridized for 4 hours at 65°C in hybridization buffer (1% BSA, 1 mM EDTA, 0.5 M NaHPO 4 pH 7.2, 7% SDS), then labeled probe was added and allowed to hybridize with the membrane overnight at 65°C. Hybridized membranes were washed twice for 10 min in wash buffer #1 (0.5% BSA, 1 mM EDTA, 40 mM NaHPO 4 pH 7.2, 5% SDS), then washed twice for 5-10 min in wash buffer #2 (1 mM EDTA, 40 mM NaHPO 4 pH 7.2, 1% SDS).
  • a labeled M. truncatula BAN probe was made using a Ready-To-Go DNA labeling beads (dCTP) kit (Amersham Pharmacia Biotech). Thirty four plants showed various levels of BAN transcripts as determined by RNA gel blot hybridization analysis (FIG. 6). Lines B-16-B, B-18-B, B-19-A, B-21-A and B-21-B had the highest levels of BAN transgene expression (FIG. 6).
  • Lines B-2-A, B-7, B-9-A, B-10, B-ll, B-13-A, B-13-B, B- 14-A, B-15-A, B-15-B, B-17-A, B-17-B, B-18-C, B-19-C, B-20-B and B-20-C had intermediate expression.
  • Gene silencing may have occurred in the multiple-copy lines B-16-A and B-19-B (FIG. 6).
  • Condensed tannins in the petals of transgenic plants were visualized by incubating fresh tissues in 1% vanillin in 5N HCI (Kristensen and Aastrup, 1986) for 30 min in petri dishes, or by staining tissues in a solution of ethanol : 6M HCI (1:1) containing 0.1% (w/v) dimethylaminocinnamaldehyde (DMACA) (Sigma) (Bavage et al. 1997) for 3-6 min, then washing three times with MilliQ water. If CTs are present a blue color develops with DMACA reagent, and the cells containing CTs can be examined under a dissecting microscope. Both vanillin and DMACA staining indicated that BAN transgenic petals contained CTs but that petals from control plants did not.
  • FIG. 8 shows DMACA staining of BAN-transgenic and control petals.
  • the white petals (after extraction of anthocyanin) were transferred to new 50 ml screw- cap tubes, washed three times in MilliQ water and then immersed in MilliQ water overnight (16 hours) in the cold room. The now semi-transparent white petals were blotted on paper tissue to remove excess water and placed into 15 ml capped tubes.
  • the absorbance of the butanol-HCl extract was measured at 550 nm (Carron et al, 1994), and cyanidin was used as standard (Giner-Chavez et al, 1997).
  • the butanol-HCl extract was also dried under vacuum and the residue re-suspended in 200 ⁇ l methanol containing 0.1% HCI for HPLC analysis.
  • the absorbance of extracts was measured at 528 nm.
  • the results are shown in Table 3, and confirm the reduction in anthocyanin levels in flowers of plants expressing M. truncatula BAN.
  • the results in Table 3 also include data on anthocyanin levels in three transgenic lines over-expressing M. truncatula dihydroflavonol reductase. In these lines, anthocyanin levels were increased. This can also be seen visually in FIG. 7, plant D-5-C.
  • the M. truncatula BAN gene has significant sequence similarity to DFR, the phenotypes resulting from over-expression of DFR or BAN are opposite, indicating that M. truncatula BAN does not possess DFR activity.
  • sorghum TC34457 and TC34925 Two barley BAN coding sequences were identified using this approach, barley 49014 and barley barley55701; as were two sorghum sequences, designated sorghum TC34457 and TC34925.
  • the corresponding coding sequences (ORFs) for the barley sequences are given in SEQ ID NO:33 and SEQ ID NO:35 and the polypeptides encoded are given in SEQ JD NO:34 and SEQ LD NO:35, respectively.
  • the coding sequences for sorghum TC34457 and sorghum TC34925 are given in SEQ ID NO:43 and SEQ ID NO:45, and the encoded polypeptides are given in SEQ JD NO:44 and SEQ JD NO:46, respectively.
  • EXAMPLE 8 Novel anthocyanidin reductase enzyme activity assay for the recombinant protein encoded by the Medicago truncatula BAN homolog and the Arabidopsis thaliana BAN cDNA clones
  • the coding region of the Medicago truncatula BAN homolog was subcloned by digesting the original plasmid with Ncol (cuts at the start codon) and Xhol (cuts after the polyA tail), then ligating the fragment into the E. coli expression vector pSE380.
  • the plasmid was used to transform E. coli BL21-Gold host cells (Stratagene), with 100 ⁇ g/ml ampicillin selection.
  • the cD ⁇ A clone of the Arabidopsis thaliana BAN was obtained as described above by RT- PCR using primers which introduced Ncol and Xbal sites at 5 1 and 3 1 (60 bp after the stop codon) of the BAN ORF, respectively.
  • the PCR products were coned into pGEM-T Easy (Promega).
  • the pGEM-T Easy-BAN plasmid was cut with Ncol and Xbal.
  • the NcoVXb ⁇ l fragment carrying the BAN ORF was purified and ligated into Ncol and Xbal cut E. coli expression vector pPROEX-1 ( GJBCO, Life
  • the ligation mix was used to transform DH5a host cells, with 100 ⁇ g/ml ampicillin selection.
  • One ml cell suspension was used to inoculate 50 ml LB medium containing ampicillin 100 ⁇ g/ml and incubated at 37°C at 250 ⁇ m until the culture density reached ODeoo ⁇ O , then incubated at 16°C or 12°C at 250 ⁇ m until the culture density reached OD 60 o 0.6 to 0.7.
  • IPTG 100 mM stock
  • the cultures were incubated an additional 20-23 hrs at the same conditions, and then the cells were collected by centrifugation at 4°C (induction at higher temperatures resulted in mostly insoluble BAN protein).
  • the pellets were used to extract enzyme or were stored at -20°C for future enzyme assays.
  • the enzyme assays were carried out in 1.5 ml polypropylene tubes containing 345 ⁇ l 100 mM Tris-HCl pH 7.0, 5 ⁇ l pelargonidin chloride, cyanidin chloride or delphinidin chloride (lOmM stock in MEOH), 50 ⁇ l NADPH (fresh 20 mM stock) and 100 ⁇ l crude enzyme extract (approximately 50 ⁇ g protein by BioRad dye-binding protein assay with BSA as a standard).
  • Initial assays were carried out with protein extracts from cultures expressing recombinant MtBAN proteins, or from cultures containing the empty expression vectors, or these extracts after boiling (boiled MtBAN protein or boiled pSE380 vector control proteins).
  • the assay mixture was mixed well and incubated in a 30 °C water bath for 30 min.
  • the reaction was stopped by adding 1 ml ethyl acetate and vortexing 1 min. Phases were separated by centrifuging at 14,000 ⁇ m 4°C for 15 min. A portion (0.8 ml) of the ethyl acetate extract (upper phase) was transferred to a new 1.5 ml tube, and the ethyl acetate was evaporated with nitrogen gas at room temperature. The residues were dissolved in 100% methanol (HPLC grade) for HPLC analysis.
  • HPLC analysis was carried out on a HP 1100 HPLC system with a UV/Nis Diode Array detector (Agilent Co., formerly Hewlett-Packard).
  • the HPLC column was a reverse phase C18 (MetaChem “Waters” Spherisorb ODS 5 urn 250 X 4.6 mm) and the solvents were 1% H 3 PO 4 (solvent A) and acetonitrile (CH 3 C ⁇ ) (solvent B).
  • the HPLC program consisted of the following percentages of CH 3 CN (B): equilibration and first 5 min after injection, 5% B; from 5 to 7 min, linear increase to 7% B; hold at 7% B until 25 min; from 25 to 40 min, linear increase to 40% B; from 40 to 40.5 min (wash cycle begins), linear increase to 95% B, hold at 95% B until 49.5 min, and linear return to 5% B (initial conditions) from 49.5 to 50 min. After a 10 min re-equilibration, the next sample was injected. The flow rate was 1.5 ml/min and the injection volume was 30 ⁇ l. Standards of ( ⁇ )-catechin or (-)-epicatechin, gallocatechin, epigallocatechin (Sigma) were used for comparison of HPLC retention times and UV diode array spectra in the assay.
  • MtBAN protein was concluded to be a novel, previously unexpected, anthocyanidin reductase, in this case reducing cyanidin to the corresponding flavan-3-ols, catechin and epicatechin, in vitro.
  • MtBAN may also act on anthocyanins (anthocyanidins with 3-glucose substitution).
  • the anthocyanidin reductase assay was repeated with extracts from cultures expressing the AtBAN (Arabidopsis) protein.
  • the protein extracts from E. coli cultures harboring the empty expression vector pPROEX-1 were used as negative controls, or these extracts after boiling.
  • protein extracts from cultures expressing the AtBAN protein were able to catalyze the reduction of cyanidin to epicatechin (FIG. 16 and FIG. 17), pelargonidin into epi-alfzelechin (FIG. 18 and FIG. 19), and delphinidin into gallocatechin (FIG. 20 and FIG. 21).
  • the lower amounts of reaction products recovered from the AtBAN reactions may be due to the fact that 4-month old frozen protein extracts were used in the assay, and additional products, like those observed with MtBAN extracts, may be observed with a more active AtBAN enzyme preparation.
  • the two product peaks generated molecular ions, fragmentation patterns and retention times matching those of the catechin and epicatechin standards, and for delphinidin as substrate, the two product peaks generated molecular ions, fragmentation patterns and retention times matching those of the gallocatechin and epigallocatechin standards.
  • pelargonidin no product standards were available for comparison, but two peaks consistent with the molecular weight of afzelechin or epi-afzelechin (16 mass units lighter than the catechin standard) were observed.
  • BAN Prior to this, BAN was thought to encode a negative regulator (transcription factor) of anthocyanin biosynthesis (Alberts, 1997).
  • the BAN gene cDNA and genomic fragments were previously cloned from Arabidopsis (Devic, 1999), but there has not been a direct demonstration of its biochemical functions with regard to condensed tannins biosynthesis, nor any previous demonstration that its over-expression or ectopic expression confers accumulation of condensed tannins in tissues that do not naturally accumulate condensed tannins.
  • the condensed tannin and anthocyanin biosynthetic pathways may interact as now described in FIG. 23, with the BAN-encoded anthocyanidin reductase (ANR) now acting upon anthocyanidins (the product of ANS, anthocyanidin synthase, or LDOX, leucoanthocyanidin oxidase), instead of competing for the leucoanthocyanidin pathway intermediates.
  • ANR anthocyanidin reductase
  • anthocyanidins the product of ANS, anthocyanidin synthase, or LDOX, leucoanthocyanidin oxidase
  • Anthocyanin (anthocyanidin-3-O-glucosides) and anthocyanidins accumulation is thus reduced by way of conversion of the anthocyanidins to flavan-3-ols.
  • Lotus corniculatus, Desmodium uncinatum and Barley cv. Morex were grown in a green house. Young leaves from L. corniculatus, unexpanded leaves, and young pods as well as open flowers and flower buds from D. uncinatum, and young grains from Barley were collected. Testa of barley grains were excised and pooled together for enzyme extraction. Mature grape fruit stored at -80°C was treated in pH 7 lOOmM Tris.HCl buffer for 30 seconds for isolated the skin for enzyme extraction.
  • Extraction buffer 1 pH7 100 mM Tris.HCl, 10% glycerol and 2 mM 1,4-dithiothreitol;
  • Extraction buffer 2 pH8 50mM phosphate buffer, 10% glycerol, 1.5% polyethyleneglycerol
  • Extraction buffer 3 ⁇ H8 100 mM Tris.HCl, 10% glycerol 1.5% polyethyleneglycerol 4000 (PEG-4000), 2mM pH 8.0 Na-DETA, 25 mM sodium ascorbate, 80 mM ⁇ -mecaptoenthanol, and 5 mM 1,4-dithiothreitol.
  • the homogenate powder of lotus leaf and barley testa tissue was suspended in 5 ml extraction buffer 1, in which 1% protenase inhibitor (Sigma) (V/V) was added.
  • the homogenate powder of flowers and pods from Desmodium were suspended in extraction buffer 2, also in which 1% protenase inhibitor (Sigma) (V/V) was added.
  • the fine powder of Desmodium leaves or grape fruit skin was respectively suspended in 6 ml or 50 ml exfraction buffer 3, in which 1% protenase inhibitor (Sigma) (V/V) is added.
  • the homogenates were votex vigorously and stayed on ice for 5-10 min, squeezed through microcloth into 50 ml tubes and then 1/5 (W/V) equilibrated Dowex 1 x 2 was added into collected squeezed mixture solution.
  • the samples were vigously votexed, and then centrifuged at 4 °C at 13000 ⁇ m (20,000 g) for 30 min.
  • the supernatants were mixed extraction buffer equilibrated polyvinylpyrrolidone (PVP) with a ratio of 1/5 (W/V) and then centrifuged at 4 °C at 14000 ⁇ m (23,000 g) for 30 min.
  • PVP polyvinylpyrrolidone
  • the supernatants were desalted on an PD-10 sephadex G-25 column (Amercia Pharmacia) equilibrated and eluted with 100 mM Tris.HCl, 2 mM DTT, 5 mM sodium ascorbate and 10% glycerol following the manufactory's protocol.
  • the desalted enzyme was concentrated with 10K MW membrane column (Amicon Ultra, MilliQ) to 0.5-1 ml for enzyme assay.
  • Enzyme assay was carried out in 200 ⁇ l in the formula of pH 7 100 mM Tris HCI, 1 mM NADPH, 100 ⁇ M cyanidin and 50-25 ⁇ g desalted crude enzyme, 30 °C for 30 min. The reaction was stopped by adding 1 ml ethyl acetate and vortexing 1 min vigorously, and then centrifuged 1 min at 10000 ⁇ m. 0.9 ml ethyl acetate extraction phase was dried with liquid nitrogen and the residues were dissolved in 50 ⁇ l methanol, of which 40 ⁇ l volume was used for HPLC assay using the same program as above (example 8).
  • FIGs. 26-29 The results of the analysis are presented in FIGs. 26-29, and show that anthocyanidin reductase from all tissues from above plants converted cyanidin into epicatechin.

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Abstract

L'invention concerne un procédé et des compositions permettant de moduler la production de tannins condensés dans des plantes. Le procédé de l'invention permet de créer des plantes présentant de nouveaux phénotypes. On peut utiliser l'expression accrue des tannins condensés dans des plantes pour augmenter la valeur nutritionnelle des plantes alimentaires à la fois pour la consommation humaine et pour la consommation animale. L'augmentation de contenu tannique condensé permet également de réduire le potentiel de ballonnement chez les animaux nourris avec certaines plantes fourragères à faible contenu en tanins condensés. L invention peut également être utilisée pour modifier la pigmentation végétale.
EP03762203A 2002-06-28 2003-06-30 Manipulation genetique de tannins condenses Expired - Lifetime EP1546335B1 (fr)

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DE60322724D1 (de) 2002-06-28 2008-09-18 Samuel Roberts Noble Found Inc Gentechnische manipulation kondensierter tannine
NZ538259A (en) * 2002-09-10 2008-03-28 Samuel Roberts Noble Found Inc Methods and compositions for production of flavonoid and isoflavonoid nutraceuticals
AU2003901797A0 (en) 2003-04-14 2003-05-01 Agresearch Limited Manipulation of condensed tannin biosynthesis
WO2005042747A2 (fr) * 2003-10-29 2005-05-12 The Samuel Roberts Noble Foundation, Inc. Hydroxylases d'isoflavonoides de plantes et leurs procedes d'utilisation
US7709701B2 (en) 2004-07-09 2010-05-04 The Samuel Roberts Noble Foundation Genetic manipulation of condensed tannins
EP2410057A1 (fr) * 2005-07-20 2012-01-25 Agriculture Victoria Services Pty Ltd Modification de la biosynthèse de flavonoïdes chez les plantes avec TT8 (Transparent Testa 8)
AU2006308510B2 (en) * 2005-10-26 2013-01-10 Agriculture Victoria Services Pty Ltd Modification of flavonoid biosynthesis in plants
CA2626920C (fr) * 2005-10-26 2018-09-18 Aidyn Mouradov Modification de la biosynthese des flavonoides dans les plantes
WO2007092934A2 (fr) * 2006-02-09 2007-08-16 The Samuel Roberts Noble Foundation, Inc. Procedes et compositions destines a modifier des voies de biosynthese de plantes
AU2008245794B2 (en) * 2007-04-26 2011-12-01 The Samuel Roberts Noble Foundation, Inc. Production of proanthocyanidins to improve forage quality
CN108410886B (zh) * 2018-02-28 2020-11-13 安徽农业大学 一种儿茶素中间体的生物合成及检测方法
WO2021126978A1 (fr) * 2019-12-17 2021-06-24 North Carolina State University Matériaux et procédés associés à des plantes transgéniques ayant des niveaux réduits d'alcaloïdes et de carcinogènes

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ATE403727T1 (de) 2008-08-15
NZ535871A (en) 2006-08-31
WO2004002215A2 (fr) 2004-01-08
DE60322724D1 (de) 2008-09-18
US7622638B2 (en) 2009-11-24
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US20040093632A1 (en) 2004-05-13
EP1546335B1 (fr) 2008-08-06

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